9-289609-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 289609
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 289609
    reference: chr 9
allele count: 4
allele frequency: 3.88961278904685e-5
allele num: 102838
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.283+28A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.265+28A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.299+28A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.404+28A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.200+28A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.200+28A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.513+28A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.200+28A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*367+28A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.200+28A>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2445
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

9-289611-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 289611
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 289611
    reference: chr 9
allele count: 5
allele frequency: 5.214199307554332e-5
allele num: 95892
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.283+30A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.200+30A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.265+30A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.404+30A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.200+30A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.200+30A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*367+30A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.513+30A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.200+30A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.299+30A>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6563
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7103
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

9-289625-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 289625
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 289625
    reference: chr 9
allele count: 3
allele frequency: 3.826628230311998e-5
allele num: 78398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.283+44T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.265+44T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.513+44T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.200+44T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*367+44T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.200+44T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.200+44T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.299+44T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.404+44T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.200+44T>C
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11383
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7679
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15296
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3471
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3085
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

9-289628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 289628
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 289628
    reference: chr 9
allele count: 2
allele frequency: 2.686583203481812e-5
allele num: 74444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*367+47A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.200+47A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.200+47A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.283+47A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.200+47A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.265+47A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.299+47A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.404+47A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.200+47A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.513+47A>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7818
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

9-304531-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304531
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304531
    reference: chr 9
allele count: 2
allele frequency: 1.672940192388122e-5
allele num: 119550
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-50C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-50C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-50C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-50C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-50C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-50C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-50C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-50C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-50C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-50C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53069
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

9-304532-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304532
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304532
    reference: chr 9
allele count: 5
allele frequency: 4.181371155229223e-5
allele num: 119578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-49C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10343
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

9-304533-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304533
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304533
    reference: chr 9
allele count: 11
allele frequency: 9.201478928613254e-5
allele num: 119546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-48G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-48G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-48G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-48G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-48G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-48G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-48G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-48G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-48G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-48G>A
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10342
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

9-304533-GCTCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304533
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304529
    reference: chr 9
allele count: 2
allele frequency: 1.672996168838773e-5
allele num: 119546
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-42_284-39delTCTC
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-42_300-39delTCTC
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-42_405-39delTCTC
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-42_201-39delTCTC
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-42_266-39delTCTC
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-42_*368-39delTCTC
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-42_514-39delTCTC
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-42_201-39delTCTC
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-42_201-39delTCTC
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-42_201-39delTCTC
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10342
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: GCTCT
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

9-304536-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304536
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304536
    reference: chr 9
allele count: 2
allele frequency: 1.672017121455324e-5
allele num: 119616
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-45C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-45C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-45C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-45C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-45C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-45C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-45C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-45C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-45C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-45C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10331
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP

9-304537-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304537
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304537
    reference: chr 9
allele count: 3
allele frequency: 2.507648327398566e-5
allele num: 119634
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-44T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-44T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-44T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-44T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-44T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-44T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-44T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-44T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-44T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-44T>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10331
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

9-304540-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304540
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304540
    reference: chr 9
allele count: 5
allele frequency: 4.179763258209055e-5
allele num: 119624
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-41C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-41C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-41C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-41C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-41C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-41C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-41C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-41C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-41C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-41C>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10328
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53077
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

9-304540-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304540
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304540
    reference: chr 9
allele count: 1
allele frequency: 8.35952651641811e-6
allele num: 119624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-41C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-41C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-41C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-41C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-41C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-41C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-41C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-41C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-41C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-41C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

9-304541-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304541
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304541
    reference: chr 9
allele count: 1
allele frequency: 8.358827757995218e-6
allele num: 119634
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-40T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-40T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-40T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-40T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-40T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-40T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-40T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-40T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-40T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-40T>C
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10326
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

9-304542-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304542
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304542
    reference: chr 9
allele count: 3
allele frequency: 2.507606406098499e-5
allele num: 119636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-39C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-39C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-39C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-39C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-39C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-39C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-39C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-39C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-39C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-39C>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10326
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

9-304543-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304543
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304543
    reference: chr 9
allele count: 1
allele frequency: 8.359107247345984e-6
allele num: 119630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-38C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-38C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-38C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-38C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-38C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-38C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-38C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-38C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-38C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-38C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

9-304546-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304546
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304546
    reference: chr 9
allele count: 1
allele frequency: 8.357290900581667e-6
allele num: 119656
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-35C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-35C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-35C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-35C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-35C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-35C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-35C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-35C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-35C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-35C>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10325
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

9-304546-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304546
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304545
    reference: chr 9
allele count: 1
allele frequency: 8.357290900581667e-6
allele num: 119656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-32delT
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-32delT
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-32delT
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-32delT
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-32delT
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-32delT
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-32delT
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-32delT
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-32delT
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-32delT
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: CT
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

9-304550-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304550
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304550
    reference: chr 9
allele count: 2
allele frequency: 1.67117884956048e-5
allele num: 119676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-31C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-31C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-31C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-31C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-31C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-31C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-31C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-31C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-31C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-31C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10325
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

9-304552-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304552
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304552
    reference: chr 9
allele count: 6
allele frequency: 5.013201430433475e-5
allele num: 119684
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-29C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-29C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-29C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-29C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-29C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-29C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-29C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-29C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-29C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-29C>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10325
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

9-304552-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304552
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304552
    reference: chr 9
allele count: 1
allele frequency: 8.355335717389125e-6
allele num: 119684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-29C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-29C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-29C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-29C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-29C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-29C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-29C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-29C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-29C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-29C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

9-304554-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304554
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304554
    reference: chr 9
allele count: 1
allele frequency: 8.355475342992263e-6
allele num: 119682
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-27C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-27C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-27C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-27C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-27C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-27C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-27C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-27C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-27C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-27C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10320
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

9-304557-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304557
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304557
    reference: chr 9
allele count: 2
allele frequency: 1.670732114812711e-5
allele num: 119708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-24C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-24C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-24C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-24C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-24C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-24C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-24C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-24C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-24C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-24C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10320
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

9-304568-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304568
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304568
    reference: chr 9
allele count: 1
allele frequency: 8.34599142032082e-6
allele num: 119818
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-13T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-13T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-13T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-13T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-13T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-13T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-13T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-13T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-13T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-13T>C
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10319
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

9-304573-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304573
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304573
    reference: chr 9
allele count: 13
allele frequency: 1.083893344894862e-4
allele num: 119938
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-8C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-8C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-8C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-8C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-8C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-8C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-8C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-8C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-8C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-8C>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10324
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 2.25e1
  variant carriers: 0
hgvs: c.405-8C>G
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

9-304574-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304574
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304574
    reference: chr 9
allele count: 2
allele frequency: 1.667361400583577e-5
allele num: 119950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.201-7A>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.201-7A>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.201-7A>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.201-7A>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.266-7A>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*368-7A>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.405-7A>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.284-7A>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.514-7A>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.300-7A>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10313
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 6.75e1
  variant carriers: 0
hgvs: c.405-7A>T
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

9-304587-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304587
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304587
    reference: chr 9
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.207A>G
  hgvsp: ENST00000487230.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.272A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*374A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.411A>G
  hgvsp: ENST00000453981.1:c.411A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.207A>G
  hgvsp: ENST00000483757.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.306A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.207A>G
  hgvsp: ENST00000469391.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.520A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.207A>G
  hgvsp: ENST00000432829.2:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.290A>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10312
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln137Gln
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/9-304591-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304591
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304591
    reference: chr 9
allele count: 1
allele frequency: 8.303165166561494e-6
allele num: 120436
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.211A>C
  hgvsp: ENSP00000417691.1:p.Ser71Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.310A>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.211A>C
  hgvsp: ENSP00000418318.1:p.Ser71Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.211A>C
  hgvsp: ENSP00000394888.2:p.Ser71Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.211A>C
  hgvsp: ENSP00000419438.1:p.Ser71Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.415A>C
  hgvsp: ENSP00000408464.1:p.Ser139Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.294A>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.276A>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*378A>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.524A>C
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10311
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser139Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

9-304597-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304597
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304597
    reference: chr 9
allele count: 1
allele frequency: 8.29393713195654e-6
allele num: 120570
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.217G>C
  hgvsp: ENSP00000419438.1:p.Glu73Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.421G>C
  hgvsp: ENSP00000408464.1:p.Glu141Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.217G>C
  hgvsp: ENSP00000417691.1:p.Glu73Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.300G>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.217G>C
  hgvsp: ENSP00000394888.2:p.Glu73Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.316G>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.217G>C
  hgvsp: ENSP00000418318.1:p.Glu73Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.282G>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*384G>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.530G>C
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10311
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2343
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu141Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

9-304604-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304604
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304604
    reference: chr 9
allele count: 7
allele frequency: 5.798638148412001e-5
allele num: 120718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*391G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.224G>T
  hgvsp: ENSP00000394888.2:p.Cys75Phe
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.323G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.224G>T
  hgvsp: ENSP00000417691.1:p.Cys75Phe
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.307G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.289G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.224G>T
  hgvsp: ENSP00000419438.1:p.Cys75Phe
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.428G>T
  hgvsp: ENSP00000408464.1:p.Cys143Phe
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.537G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.224G>T
  hgvsp: ENSP00000418318.1:p.Cys75Phe
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10315
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Cys143Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/9-304608-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304608
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304608
    reference: chr 9
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.228C>A
  hgvsp: ENST00000487230.1:c.228C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.228C>A
  hgvsp: ENST00000469391.1:c.228C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.327C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.293C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.311C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*395C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.432C>A
  hgvsp: ENST00000453981.1:c.432C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.228C>A
  hgvsp: ENST00000432829.2:c.228C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.228C>A
  hgvsp: ENST00000483757.1:c.228C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.541C>A
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10310
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly144Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

9-304612-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304612
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304612
    reference: chr 9
allele count: 1
allele frequency: 8.276775368316504e-6
allele num: 120820
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.297A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.315A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.232A>G
  hgvsp: ENSP00000417691.1:p.Lys78Glu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.232A>G
  hgvsp: ENSP00000418318.1:p.Lys78Glu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.436A>G
  hgvsp: ENSP00000408464.1:p.Lys146Glu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.545A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.331A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.232A>G
  hgvsp: ENSP00000419438.1:p.Lys78Glu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.232A>G
  hgvsp: ENSP00000394888.2:p.Lys78Glu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*399A>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10309
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys146Glu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

9-304621-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304621
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304621
    reference: chr 9
allele count: 1
allele frequency: 8.269656974628692e-6
allele num: 120924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.241G>A
  hgvsp: ENSP00000418318.1:p.Gly81Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.241G>A
  hgvsp: ENSP00000419438.1:p.Gly81Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.324G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.241G>A
  hgvsp: ENSP00000394888.2:p.Gly81Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.340G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.554G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.241G>A
  hgvsp: ENSP00000417691.1:p.Gly81Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.445G>A
  hgvsp: ENSP00000408464.1:p.Gly149Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.306G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*408G>A
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10309
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly149Arg
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

9-304623-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304623
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304623
    reference: chr 9
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.243A>G
  hgvsp: ENST00000487230.1:c.243A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.243A>G
  hgvsp: ENST00000432829.2:c.243A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.243A>G
  hgvsp: ENST00000483757.1:c.243A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*410A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.556A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.342A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.447A>G
  hgvsp: ENST00000453981.1:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.243A>G
  hgvsp: ENST00000469391.1:c.243A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.308A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.326A>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10309
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly149Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

9-304627-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304627
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304627
    reference: chr 9
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.247C>T
  hgvsp: ENSP00000418318.1:p.Arg83Ter
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.247C>T
  hgvsp: ENSP00000417691.1:p.Arg83Ter
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.247C>T
  hgvsp: ENSP00000394888.2:p.Arg83Ter
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.312C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.346C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.247C>T
  hgvsp: ENSP00000419438.1:p.Arg83Ter
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.451C>T
  hgvsp: ENSP00000408464.1:p.Arg151Ter
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.560C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*414C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.330C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg151Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

9-304628-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304628
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304628
    reference: chr 9
allele count: 175
allele frequency: 1.446257086659725e-3
allele num: 121002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.347G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.248G>A
  hgvsp: ENSP00000417691.1:p.Arg83Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.248G>A
  hgvsp: ENSP00000394888.2:p.Arg83Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.248G>A
  hgvsp: ENSP00000418318.1:p.Arg83Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*415G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.248G>A
  hgvsp: ENSP00000419438.1:p.Arg83Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.561G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.313G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.452G>A
  hgvsp: ENSP00000408464.1:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.331G>A
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5061
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10359
  bin: 9.75e1
  variant carriers: 163
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg151Gln
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

9-304641-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304641
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304641
    reference: chr 9
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*428C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.326C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.261C>G
  hgvsp: ENSP00000419438.1:p.His87Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.344C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.261C>G
  hgvsp: ENSP00000394888.2:p.His87Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.465C>G
  hgvsp: ENSP00000408464.1:p.His155Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.261C>G
  hgvsp: ENSP00000418318.1:p.His87Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.261C>G
  hgvsp: ENSP00000417691.1:p.His87Gln
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.574C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.360C>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10226
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53063
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His155Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

9-304646-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304646
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304646
    reference: chr 9
allele count: 76
allele frequency: 6.273836450989781e-4
allele num: 121138
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.579C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*433C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.266C>T
  hgvsp: ENSP00000419438.1:p.Thr89Met
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.266C>T
  hgvsp: ENSP00000417691.1:p.Thr89Met
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.266C>T
  hgvsp: ENSP00000418318.1:p.Thr89Met
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.331C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.365C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.266C>T
  hgvsp: ENSP00000394888.2:p.Thr89Met
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.470C>T
  hgvsp: ENSP00000408464.1:p.Thr157Met
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.349C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10251
  bin: 9.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr157Met
num of homozygotes: 6
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-304647-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304647
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304647
    reference: chr 9
allele count: 3
allele frequency: 2.476309967973058e-5
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.580G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.267G>A
  hgvsp: ENST00000487230.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.471G>A
  hgvsp: ENST00000453981.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.267G>A
  hgvsp: ENST00000483757.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.267G>A
  hgvsp: ENST00000469391.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*434G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.332G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.267G>A
  hgvsp: ENST00000432829.2:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.350G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.366G>A
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10211
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5511
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr157Thr
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

9-304648-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304648
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304648
    reference: chr 9
allele count: 5
allele frequency: 4.126978886376017e-5
allele num: 121154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.351C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.268C>G
  hgvsp: ENSP00000394888.2:p.Leu90Val
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.333C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.472C>G
  hgvsp: ENSP00000408464.1:p.Leu158Val
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.268C>G
  hgvsp: ENSP00000418318.1:p.Leu90Val
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.367C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.581C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.268C>G
  hgvsp: ENSP00000417691.1:p.Leu90Val
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.268C>G
  hgvsp: ENSP00000419438.1:p.Leu90Val
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*435C>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5511
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10210
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu158Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

9-304652-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304652
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304652
    reference: chr 9
allele count: 7
allele frequency: 5.776435444207885e-5
allele num: 121182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.272C>T
  hgvsp: ENSP00000419438.1:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.272C>T
  hgvsp: ENSP00000418318.1:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.355C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.337C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.585C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.371C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.272C>T
  hgvsp: ENSP00000394888.2:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.476C>T
  hgvsp: ENSP00000408464.1:p.Pro159Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*439C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.272C>T
  hgvsp: ENSP00000417691.1:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10207
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro159Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

9-304653-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304653
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304653
    reference: chr 9
allele count: 19
allele frequency: 1.567734376289255e-4
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.338G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.477G>A
  hgvsp: ENST00000453981.1:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.586G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.356G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.273G>A
  hgvsp: ENST00000469391.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.273G>A
  hgvsp: ENST00000487230.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.273G>A
  hgvsp: ENST00000483757.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.273G>A
  hgvsp: ENST00000432829.2:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*440G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.372G>A
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10207
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro159Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

9-304657-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304657
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304655
    reference: chr 9
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.483_484delGA
  hgvsp: ENSP00000408464.1:p.Gln161HisfsTer3
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.279_280delGA
  hgvsp: ENSP00000417691.1:p.Gln93HisfsTer3
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.279_280delGA
  hgvsp: ENSP00000419438.1:p.Gln93HisfsTer3
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.362_363delGA
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.279_280delGA
  hgvsp: ENSP00000418318.1:p.Gln93HisfsTer3
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.279_280delGA
  hgvsp: ENSP00000394888.2:p.Gln93HisfsTer3
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.592_593delGA
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.378_379delGA
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*446_*447delGA
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.344_345delGA
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10190
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln161HisfsTer3
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: CAG
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

9-304661-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304661
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304661
    reference: chr 9
allele count: 4
allele frequency: 3.299350028044475e-5
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.281C>T
  hgvsp: ENSP00000417691.1:p.Thr94Met
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.364C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.485C>T
  hgvsp: ENSP00000408464.1:p.Thr162Met
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.281C>T
  hgvsp: ENSP00000394888.2:p.Thr94Met
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.380C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.281C>T
  hgvsp: ENSP00000418318.1:p.Thr94Met
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.281C>T
  hgvsp: ENSP00000419438.1:p.Thr94Met
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.346C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.594C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*448C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10190
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53059
  bin: 9.75e1
  variant carriers: 4
hgvs: p.Thr162Met
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

9-304662-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304662
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304662
    reference: chr 9
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.282G>A
  hgvsp: ENST00000487230.1:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.347G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*449G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.381G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.282G>A
  hgvsp: ENST00000432829.2:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.282G>A
  hgvsp: ENST00000483757.1:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.595G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.486G>A
  hgvsp: ENST00000453981.1:c.486G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.282G>A
  hgvsp: ENST00000469391.1:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.365G>A
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10188
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr162Thr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

9-304665-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304665
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304665
    reference: chr 9
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.285T>A
  hgvsp: ENSP00000417691.1:p.Phe95Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.368T>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.598T>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.285T>A
  hgvsp: ENSP00000419438.1:p.Phe95Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.285T>A
  hgvsp: ENSP00000394888.2:p.Phe95Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.489T>A
  hgvsp: ENSP00000408464.1:p.Phe163Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.285T>A
  hgvsp: ENSP00000418318.1:p.Phe95Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.350T>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*452T>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.384T>A
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10187
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe163Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

9-304668-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304668
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304668
    reference: chr 9
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.288G>C
  hgvsp: ENSP00000419438.1:p.Glu96Asp
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.288G>C
  hgvsp: ENSP00000417691.1:p.Glu96Asp
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.371G>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.492G>C
  hgvsp: ENSP00000408464.1:p.Glu164Asp
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.288G>C
  hgvsp: ENSP00000418318.1:p.Glu96Asp
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.601G>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.353G>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*455G>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.288G>C
  hgvsp: ENSP00000394888.2:p.Glu96Asp
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.387G>C
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu164Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

9-304670-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304670
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304670
    reference: chr 9
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.603C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*457C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.290C>G
  hgvsp: ENSP00000394888.2:p.Ser97Trp
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.494C>G
  hgvsp: ENSP00000408464.1:p.Ser165Trp
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.290C>G
  hgvsp: ENSP00000418318.1:p.Ser97Trp
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.355C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.373C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.290C>G
  hgvsp: ENSP00000419438.1:p.Ser97Trp
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.389C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.290C>G
  hgvsp: ENSP00000417691.1:p.Ser97Trp
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5515
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser165Trp
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

9-304670-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304670
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304670
    reference: chr 9
allele count: 65
allele frequency: 5.359763840559395e-4
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*457C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.290C>T
  hgvsp: ENSP00000417691.1:p.Ser97Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.494C>T
  hgvsp: ENSP00000408464.1:p.Ser165Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.290C>T
  hgvsp: ENSP00000394888.2:p.Ser97Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.355C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.290C>T
  hgvsp: ENSP00000418318.1:p.Ser97Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.389C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.603C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.290C>T
  hgvsp: ENSP00000419438.1:p.Ser97Leu
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.373C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5515
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 9.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2714
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser165Leu
num of homozygotes: 1
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-304676-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304676
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304676
    reference: chr 9
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.361C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.395C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*463C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.609C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.296C>A
  hgvsp: ENSP00000418318.1:p.Thr99Asn
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.500C>A
  hgvsp: ENSP00000408464.1:p.Thr167Asn
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.296C>A
  hgvsp: ENSP00000417691.1:p.Thr99Asn
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.296C>A
  hgvsp: ENSP00000394888.2:p.Thr99Asn
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.379C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.296C>A
  hgvsp: ENSP00000419438.1:p.Thr99Asn
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr167Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

9-304677-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304677
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304677
    reference: chr 9
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.297C>G
  hgvsp: ENST00000483757.1:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.501C>G
  hgvsp: ENST00000453981.1:c.501C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*464C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.297C>G
  hgvsp: ENST00000469391.1:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.396C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.380C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.297C>G
  hgvsp: ENST00000487230.1:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.362C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.297C>G
  hgvsp: ENST00000432829.2:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.610C>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr167Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

9-304688-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304688
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304688
    reference: chr 9
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.308G>T
  hgvsp: ENSP00000394888.2:p.Ser103Ile
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.373G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.308G>T
  hgvsp: ENSP00000419438.1:p.Ser103Ile
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.308G>T
  hgvsp: ENSP00000417691.1:p.Ser103Ile
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.512G>T
  hgvsp: ENSP00000408464.1:p.Ser171Ile
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.391G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.308G>T
  hgvsp: ENSP00000418318.1:p.Ser103Ile
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.621G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*475G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.407G>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser171Ile
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

9-304694-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304694
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304694
    reference: chr 9
allele count: 4
allele frequency: 3.29777235477435e-5
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.314C>G
  hgvsp: ENSP00000394888.2:p.Pro105Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.397C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.413C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.627C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.379C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.314C>G
  hgvsp: ENSP00000417691.1:p.Pro105Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.314C>G
  hgvsp: ENSP00000418318.1:p.Pro105Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.314C>G
  hgvsp: ENSP00000419438.1:p.Pro105Arg
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*481C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.518C>G
  hgvsp: ENSP00000408464.1:p.Pro173Arg
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10146
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro173Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

9-304695-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304695
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304695
    reference: chr 9
allele count: 4
allele frequency: 3.297826732183491e-5
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.414C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.398C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.315C>G
  hgvsp: ENST00000487230.1:c.315C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.519C>G
  hgvsp: ENST00000453981.1:c.519C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.315C>G
  hgvsp: ENST00000469391.1:c.315C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.315C>G
  hgvsp: ENST00000432829.2:c.315C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.315C>G
  hgvsp: ENST00000483757.1:c.315C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.628C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.380C>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*482C>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10143
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro173Pro
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

9-304695-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304695
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304695
    reference: chr 9
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.315C>T
  hgvsp: ENST00000483757.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.519C>T
  hgvsp: ENST00000453981.1:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.380C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.628C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.315C>T
  hgvsp: ENST00000432829.2:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.398C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.315C>T
  hgvsp: ENST00000469391.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.315C>T
  hgvsp: ENST00000487230.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.414C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*482C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10143
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro173Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/9-304703-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304703
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304703
    reference: chr 9
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.323A>C
  hgvsp: ENSP00000417691.1:p.Gln108Pro
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*490A>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.323A>C
  hgvsp: ENSP00000419438.1:p.Gln108Pro
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.406A>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000418318
  ensembl transcript: ENST00000487230
  gene symbol: DOCK8
  hgvsc: ENST00000487230.1:c.323A>C
  hgvsp: ENST00000487230.1:c.323A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.636A>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.422A>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.388A>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.323A>C
  hgvsp: ENSP00000394888.2:p.Gln108Pro
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.527A>C
  hgvsp: ENSP00000408464.1:p.Gln176Pro
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln176Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

9-304710-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304710
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304710
    reference: chr 9
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+6T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+6T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+6T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+6T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+6T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+6T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+6T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+6T>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+6T>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10138
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2673
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
hgvs: c.528+6T>G
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/9-304711-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304711
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304711
    reference: chr 9
allele count: 74
allele frequency: 6.101080056063979e-4
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+7C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+7C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+7C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+7C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+7C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+7C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+7C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+7C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+7C>A
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10147
  bin: 9.75e1
  variant carriers: 43
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
hgvs: c.528+7C>A
num of homozygotes: 2
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

9-304717-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304717
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304717
    reference: chr 9
allele count: 424
allele frequency: 3.495869267681348e-3
allele num: 121286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+13A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+13A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+13A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+13A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+13A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+13A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+13A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+13A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+13A>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 9.75e1
  variant carriers: 242
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 7.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 9.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 4
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

9-304718-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304718
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304718
    reference: chr 9
allele count: 2
allele frequency: 1.649049323065253e-5
allele num: 121282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+14A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+14A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+14A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+14A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+14A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+14A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+14A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+14A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+14A>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9979
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-304719-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304719
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304719
    reference: chr 9
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+15C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+15C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+15C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+15C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+15C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+15C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+15C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+15C>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+15C>A
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2611
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

9-304721-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304721
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304721
    reference: chr 9
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+17A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+17A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+17A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+17A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+17A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+17A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+17A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+17A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+17A>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9979
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

9-304727-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304727
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304727
    reference: chr 9
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+23G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+23G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+23G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+23G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+23G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+23G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+23G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+23G>A
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+23G>A
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

9-304739-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304739
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304739
    reference: chr 9
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+35C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+35C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+35C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+35C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+35C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+35C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+35C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+35C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+35C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53036
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

9-304740-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304740
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304740
    reference: chr 9
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+36T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+36T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+36T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+36T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+36T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+36T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+36T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+36T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+36T>C
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2198
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

9-304745-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304745
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304745
    reference: chr 9
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+41T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+41T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+41T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+41T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+41T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+41T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+41T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+41T>C
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+41T>C
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

9-304751-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304751
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304751
    reference: chr 9
allele count: 2
allele frequency: 1.649457328538911e-5
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+47G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+47G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+47G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+47G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+47G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+47G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+47G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+47G>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+47G>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

9-304752-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304752
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304752
    reference: chr 9
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+48C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+48C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+48C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+48C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+48C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+48C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+48C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+48C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+48C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9977
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

9-304753-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 304753
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 304753
    reference: chr 9
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*491+49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.528+49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.407+49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.637+49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.324+49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.324+49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.324+49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.423+49C>T
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.389+49C>T
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9977
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

9-311911-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 311911
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 311911
    reference: chr 9
allele count: 1
allele frequency: 8.407741848694278e-6
allele num: 118938
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000394888
  ensembl transcript: ENST00000432829
  gene symbol: DOCK8
  hgvsc: ENST00000432829.2:c.325-43A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000436628
  ensembl transcript: ENST00000524396
  gene symbol: DOCK8
  hgvsc: ENST00000524396.1:c.*492-43A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000382341
  gene symbol: DOCK8
  hgvsc: ENST00000382341.1:n.424-43A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000478380
  gene symbol: DOCK8
  hgvsc: ENST00000478380.1:n.408-43A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000417691
  ensembl transcript: ENST00000483757
  gene symbol: DOCK8
  hgvsc: ENST00000483757.1:c.325-43A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000454469
  gene symbol: DOCK8
  hgvsc: ENST00000454469.2:n.638-43A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl transcript: ENST00000495184
  gene symbol: DOCK8
  hgvsc: ENST00000495184.1:n.390-43A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000419438
  ensembl transcript: ENST00000469391
  gene symbol: DOCK8
  hgvsc: ENST00000469391.1:c.325-43A>G
  variant of: http://identifiers.org/hgnc/19191
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107099
  ensembl protein: ENSP00000408464
  ensembl transcript: ENST00000453981
  gene symbol: DOCK8
  hgvsc: ENST00000453981.1:c.529-43A>G
  variant of: http://identifiers.org/hgnc/19191
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28354
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 21701
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2844
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4620
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14428
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2796
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7513
bin: 9.75e1
variant carriers: 4

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5674
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.701514542286557e-5
allele num: 14922
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.589246617135063e-5
allele num: 55722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6876
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

QD
type: SiteQuality
SIO_000300: 1.614e1

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

DP
type: SiteQuality
SIO_000300: 1.524916e6

GenotypeQuality
all individuals: 459
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3433
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3332
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20756
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7514
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 10166
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14308
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.9573666468372e-4
allele num: 10086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51922
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5234
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7730
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

FS
type: SiteQuality
SIO_000300: 3.953e0

MQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

QD
type: SiteQuality
SIO_000300: 2.212e1

VQSLOD
type: SiteQuality
SIO_000300: -2.144e0

DP
type: SiteQuality
SIO_000300: 1.406633e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.01e-1

MQ
type: SiteQuality
SIO_000300: 5.914e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.26e-2

GenotypeQuality
all individuals: 1868
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5354
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10177
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3638
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1169
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13925
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1481
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7510
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 242
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 458
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41984
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.306273062730627e-4
allele num: 13008
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.211371e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.06e-2

FS
type: SiteQuality
SIO_000300: 5.568e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e0

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.456e1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

GenotypeQuality
all individuals: 3549
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1650
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9704
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11659
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2152
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7510
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3143
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3130
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.564700359881083e-4
allele num: 12782
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8658
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39660
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.254e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.24e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: -1.246e-1

DP
type: SiteQuality
SIO_000300: 1.19478e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.57e0

GenotypeQuality
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.032140691328078e-5
allele num: 65960
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.434e1

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.683e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 4.349649e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

GenotypeQuality
all individuals: 425
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53080
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.214329083181542e-4
allele num: 16470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.030854094683882e-5
allele num: 65988
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 2.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e-1

FS
type: SiteQuality
SIO_000300: 4.531e0

DP
type: SiteQuality
SIO_000300: 4.349624e6

MQ
type: SiteQuality
SIO_000300: 5.991e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 1.28e1

GenotypeQuality
all individuals: 236
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53068
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 874
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 826
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 3.091508656224237e-4
allele num: 9704
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: 6
allele frequency: 9.095870474804439e-5
allele num: 65964
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.741250217656277e-4
allele num: 11486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

DP
type: SiteQuality
SIO_000300: 4.350143e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.73e-1

FS
type: SiteQuality
SIO_000300: 4.159e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.474e1

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 2.25e1
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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53068
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.031956824934813e-5
allele num: 65964
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 4.159e0

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 4.350143e6

MQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e0

QD
type: SiteQuality
SIO_000300: 1.474e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.73e-1

GenotypeQuality
all individuals: 423
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.214329083181542e-4
allele num: 16470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
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: 65994
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 2.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

FS
type: SiteQuality
SIO_000300: 5.365e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.736e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.291e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 4.349093e6

GenotypeQuality
all individuals: 505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53074
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 836
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 170
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variant carriers: 0

GenotypeQuality
all individuals: 425
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variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.545041359876375e-5
allele num: 66006
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.706e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.352e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.349288e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.02e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
all individuals: 122
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
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variant carriers: 0

GenotypeQuality
all individuals: 428
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variant carriers: 0

GenotypeQuality
all individuals: 888
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variant carriers: 0

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

GenotypeQuality
all individuals: 503
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
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variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.140859551717047e-4
allele num: 9726
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65998
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

DP
type: SiteQuality
SIO_000300: 4.349653e6

FS
type: SiteQuality
SIO_000300: 9.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

MQ
type: SiteQuality
SIO_000300: 5.991e1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 1.558e1

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53077
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515197430225158e-5
allele num: 65998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 1.558e1

FS
type: SiteQuality
SIO_000300: 9.86e-1

MQ
type: SiteQuality
SIO_000300: 5.991e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

DP
type: SiteQuality
SIO_000300: 4.349653e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

GenotypeQuality
all individuals: 230
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53076
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 135
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GenotypeQuality
all individuals: 118
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GenotypeQuality
all individuals: 503
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GenotypeQuality
all individuals: 91
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GenotypeQuality
all individuals: 115
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GenotypeQuality
all individuals: 426
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variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 52
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GenotypeQuality
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GenotypeQuality
all individuals: 1029
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 164
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
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GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514921981517952e-5
allele num: 66010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.307e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.96e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.75e-1

DP
type: SiteQuality
SIO_000300: 4.349436e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 503
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GenotypeQuality
all individuals: 888
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.740341106856944e-4
allele num: 11492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66010
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.349552e6

FS
type: SiteQuality
SIO_000300: 4.556e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.642e1

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

GenotypeQuality
all individuals: 53074
bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 108
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GenotypeQuality
all individuals: 840
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GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 166
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GenotypeQuality
all individuals: 233
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GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 443
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GenotypeQuality
all individuals: 130
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GenotypeQuality
all individuals: 1031
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GenotypeQuality
all individuals: 426
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GenotypeQuality
all individuals: 889
bin: 8.25e1
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GenotypeQuality
all individuals: 503
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1669
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66010
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9720
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.274e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

VQSLOD
type: SiteQuality
SIO_000300: -1.82e0

DP
type: SiteQuality
SIO_000300: 4.349529e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.997e1

MQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.22e-1

GenotypeQuality
all individuals: 428
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514600751241973e-5
allele num: 66024
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.85e0

FS
type: SiteQuality
SIO_000300: 2.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.74e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.454e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 4.349952e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e-1

GenotypeQuality
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bin: 7.5e0
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514600751241973e-5
allele num: 66024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.74e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e-1

FS
type: SiteQuality
SIO_000300: 2.93e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: 2.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

DP
type: SiteQuality
SIO_000300: 4.349952e6

QD
type: SiteQuality
SIO_000300: 1.454e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.028467595396729e-5
allele num: 66040
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 4.350645e6

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

QD
type: SiteQuality
SIO_000300: 1.41e1

FS
type: SiteQuality
SIO_000300: 1.533e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.654e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1033
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.643429681807141e-4
allele num: 16468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
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: 66042
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.554e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 4.351339e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

GenotypeQuality
all individuals: 130
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.027115858668858e-4
allele num: 9736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66042
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 4.351339e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.554e1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66042
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.076e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.351085e6

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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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
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Other
type: Population
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66066
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African
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allele count: 2
allele frequency: 2.054231717337716e-4
allele num: 9736
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8464
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FS
type: SiteQuality
SIO_000300: 6.67e-1

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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QD
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MQRankSum
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ClippingRankSum
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DP
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66116
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 896
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East Asian
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allele count: 1
allele frequency: 1.180358829084042e-4
allele num: 8472
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VQSLOD
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MQRankSum
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FS
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SIO_000300: 6.091e0

ClippingRankSum
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SIO_000300: -1.495e0

MQ
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SIO_000300: 5.927e1

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: 9.409999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.526e1

DP
type: SiteQuality
SIO_000300: 4.353411e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

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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bin: 9.25e1
variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Latino
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allele count: 13
allele frequency: 1.131221719457014e-3
allele num: 11492
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9818
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66188
num of homozygotes: 0

VQSLOD
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QD
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FS
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InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: -4.044e0

ReadPosRankSum
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SIO_000300: 6.43e-1

MQRankSum
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SIO_000300: 7.6e-2

MQ
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SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

DP
type: SiteQuality
SIO_000300: 4.356031e6

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

African
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allele count: 1
allele frequency: 1.017915309446254e-4
allele num: 9824
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510756586898719e-5
allele num: 66192
num of homozygotes: 0

MQRankSum
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SIO_000300: 1.05e0

VQSLOD
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SIO_000300: 6.53e-1

DP
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InbreedingCoeff
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QD
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BaseQRankSum
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SIO_000300: 2.22e0

ReadPosRankSum
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SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 4.637e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

ClippingRankSum
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SIO_000300: -5.25e-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

Other
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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
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num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.986019572598362e-5
allele num: 10014
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

DP
type: SiteQuality
SIO_000300: 4.358566e6

FS
type: SiteQuality
SIO_000300: 6.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
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African
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allele count: 1
allele frequency: 9.930486593843098e-5
allele num: 10070
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.97e-1

BaseQRankSum
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SIO_000300: -1.224e0

QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: 2.74e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
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MQRankSum
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.2e-2

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66440
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African
type: Population
allele count: 1
allele frequency: 9.869719699960521e-5
allele num: 10132
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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QD
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7
allele frequency: 1.052789893217025e-4
allele num: 66490
num of homozygotes: 0

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

Other
type: Population
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African
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South Asian
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
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allele num: 11506
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

MQRankSum
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ReadPosRankSum
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MQ
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DP
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FS
type: SiteQuality
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BaseQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.170411985018727e-4
allele num: 8544
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.365e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.25e0

DP
type: SiteQuality
SIO_000300: 4.363017e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.437e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.86e0

MQRankSum
type: SiteQuality
SIO_000300: -5.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.935e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.48e1

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169043722235212e-4
allele num: 8554
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
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: 6598
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e0

FS
type: SiteQuality
SIO_000300: 3.547e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.12e1

DP
type: SiteQuality
SIO_000300: 4.364106e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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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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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2527
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
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: 8556
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.364072e6

QD
type: SiteQuality
SIO_000300: 1.133e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.632e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

MQ
type: SiteQuality
SIO_000300: 5.99e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.703085581214826e-5
allele num: 10306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.364521e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.05e0

VQSLOD
type: SiteQuality
SIO_000300: -4.347e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.067e0

MQRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

FS
type: SiteQuality
SIO_000300: 6.008e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.364e1

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
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GenotypeQuality
all individuals: 890
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GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 956
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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: 175

GenotypeQuality
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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: 11
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.937608990505716e-4
allele num: 10322
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 9.099733074496481e-4
allele num: 16484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 149
allele frequency: 2.237371613910745e-3
allele num: 66596
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.500583430571762e-4
allele num: 8570
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.338771259979174e-4
allele num: 11524
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

FS
type: SiteQuality
SIO_000300: 5.19e-1

QD
type: SiteQuality
SIO_000300: 1.285e1

DP
type: SiteQuality
SIO_000300: 4.386469e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.94e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2604
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 17
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.134e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: 1.4e-2

BaseQRankSum
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SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.169e1

DP
type: SiteQuality
SIO_000300: 4.359211e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.936e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.63e-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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bin: 9.75e1
variant carriers: 70

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

South Asian
type: Population
allele count: 71
allele frequency: 4.305639781685871e-3
allele num: 16490
num of homozygotes: 6

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000930288389401e-5
allele num: 66646
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.734003814808393e-4
allele num: 11534
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-2

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.366543e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

FS
type: SiteQuality
SIO_000300: 1.745e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.102e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-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
all individuals: 16
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GenotypeQuality
all individuals: 7
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variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.895752895752896e-4
allele num: 10360
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: 8598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 4.023e1

DP
type: SiteQuality
SIO_000300: 4.358574e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.32e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.483e0

QD
type: SiteQuality
SIO_000300: 1.305e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.501650363079878e-5
allele num: 66652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.14e1

InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
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SIO_000300: 5.959e1

MQRankSum
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SIO_000300: 2.56e-1

FS
type: SiteQuality
SIO_000300: 1.891e0

BaseQRankSum
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SIO_000300: -2.753e0

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-1

DP
type: SiteQuality
SIO_000300: 4.358851e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e-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

African
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allele count: 2
allele frequency: 1.928640308582449e-4
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
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: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.001320290463902e-5
allele num: 66652
num of homozygotes: 0

QD
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BaseQRankSum
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SIO_000300: 3.52e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.25e-1

VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.142e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.65e-1

DP
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SIO_000300: 4.358881e6

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 18
allele frequency: 1.559251559251559e-3
allele num: 11544
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.56e-1

MQRankSum
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SIO_000300: -1.48e-1

QD
type: SiteQuality
SIO_000300: 1.273e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.86e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.183e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 4.360319e6

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
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South Asian
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allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.357587e6

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.352e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.946e1

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

VQSLOD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 9.637625289128758e-5
allele num: 10376
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.999760019198464e-5
allele num: 66672
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

InbreedingCoeff
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DP
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ReadPosRankSum
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QD
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VQSLOD
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FS
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MQ
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MQRankSum
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BaseQRankSum
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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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
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ClippingRankSum
type: SiteQuality
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FS
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MQRankSum
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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BaseQRankSum
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
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African
type: Population
allele count: 0
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Other
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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MQRankSum
type: SiteQuality
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FS
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VQSLOD
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QD
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 4.357569e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

MQRankSum
type: SiteQuality
SIO_000300: 8.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.949e0

QD
type: SiteQuality
SIO_000300: 1.307e1

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 75
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

BaseQRankSum
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SIO_000300: 2.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.65e-1

DP
type: SiteQuality
SIO_000300: 4.363034e6

FS
type: SiteQuality
SIO_000300: 5.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.34e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 64

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 482
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 60
allele frequency: 8.997120921305183e-4
allele num: 66688
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.889060092449923e-4
allele num: 10384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

FS
type: SiteQuality
SIO_000300: 5.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

QD
type: SiteQuality
SIO_000300: 1.34e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 4.363034e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.65e-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
all individuals: 13
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.076e0

VQSLOD
type: SiteQuality
SIO_000300: -4.11e-1

DP
type: SiteQuality
SIO_000300: 4.355029e6

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.083e0

QD
type: SiteQuality
SIO_000300: 1.227e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.01e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.090000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.429e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.035e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.43e-1

DP
type: SiteQuality
SIO_000300: 4.355048e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
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: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.83e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.68e-1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 3.254e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.354932e6

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.049606775559589e-4
allele num: 6612
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: 8626
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.354757e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

QD
type: SiteQuality
SIO_000300: 1.443e1

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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bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

East Asian
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allele count: 4
allele frequency: 4.63821892393321e-4
allele num: 8624
num of homozygotes: 0

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

FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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DP
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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SIO_000300: -3.23e-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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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
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: 8624
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 2.112e0

MQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.96e0

QD
type: SiteQuality
SIO_000300: 1.261e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.92e-1

DP
type: SiteQuality
SIO_000300: 4.354538e6

GenotypeDepth
all individuals: 2542
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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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bin: 4.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 7.75e1
variant carriers: 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: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.115e0

DP
type: SiteQuality
SIO_000300: 4.354084e6

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.49e1

VQSLOD
type: SiteQuality
SIO_000300: 5.49e-1

FS
type: SiteQuality
SIO_000300: 8.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.23e-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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 474
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
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: 16500
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.353597e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.23e0

MQ
type: SiteQuality
SIO_000300: 5.867e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.007e0

FS
type: SiteQuality
SIO_000300: 4.347e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.317e0

QD
type: SiteQuality
SIO_000300: 1.363e1

GenotypeQuality
all individuals: 950
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 71

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
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variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 7
allele frequency: 6.053268765133172e-4
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 65
allele frequency: 6.256015399422521e-3
allele num: 10390
num of homozygotes: 2

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99868058054456e-5
allele num: 66696
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.46e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.45e-2

QD
type: SiteQuality
SIO_000300: 1.347e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.049e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.99e-1

DP
type: SiteQuality
SIO_000300: 4.355026e6

GenotypeQuality
all individuals: 935
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variant carriers: 0

GenotypeQuality
all individuals: 470
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variant carriers: 0

GenotypeQuality
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variant carriers: 419

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 25
allele frequency: 2.161881701833276e-3
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.496926260233305e-5
allele num: 66694
num of homozygotes: 0

African
type: Population
allele count: 391
allele frequency: 3.763233878729547e-2
allele num: 10390
num of homozygotes: 4

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

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

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

QD
type: SiteQuality
SIO_000300: 1.524e1

FS
type: SiteQuality
SIO_000300: 7.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.26e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e0

VQSLOD
type: SiteQuality
SIO_000300: 4.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

DP
type: SiteQuality
SIO_000300: 4.357085e6

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 12
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 4.340074e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.452e1

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

FS
type: SiteQuality
SIO_000300: 6.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.14e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.65e-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
all individuals: 517
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.843e1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.295e1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 876
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GenotypeQuality
all individuals: 2452
bin: 6.25e1
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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: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

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

MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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FS
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ClippingRankSum
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DP
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VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.216e1

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66684
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African
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allele num: 10388
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South Asian
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Other
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allele frequency: 0.0e0
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Latino
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DP
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ClippingRankSum
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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BaseQRankSum
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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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South Asian
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allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.159823706796567e-4
allele num: 8622
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.843e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 4.335917e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 66682
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.212e1

VQSLOD
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InbreedingCoeff
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SIO_000300: -3.0e-4

BaseQRankSum
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SIO_000300: -1.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.99e0

FS
type: SiteQuality
SIO_000300: 6.513e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.03e-1

DP
type: SiteQuality
SIO_000300: 4.335148e6

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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African
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allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.999580058791769e-5
allele num: 66676
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
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InbreedingCoeff
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DP
type: SiteQuality
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MQRankSum
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QD
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.89e-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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South Asian
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allele num: 16500
num of homozygotes: 0

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

Latino
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East Asian
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European (Finnish)
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Other
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South Asian
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African
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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VQSLOD
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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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