9-35103129-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35103129
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35103129
    reference: chr 9
allele count: 1
allele frequency: 8.616975441619991e-6
allele num: 116050
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165283
  ensembl protein: ENSP00000348886
  ensembl transcript: ENST00000356493
  gene symbol: STOML2
  hgvsc: ENST00000356493.5:c.-38C>T
  variant of: http://identifiers.org/hgnc/14559
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165283
  ensembl protein: ENSP00000395743
  ensembl transcript: ENST00000452248
  gene symbol: STOML2
  hgvsc: ENST00000452248.2:c.-38C>T
  variant of: http://identifiers.org/hgnc/14559
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1847
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3358
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13004
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4520
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11889
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6577
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4144
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16254
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

9-35103130-AGCGGAGCGGTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35103130
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35103119
    reference: chr 9
allele count: 1
allele frequency: 8.608370779746225e-6
allele num: 116166
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165283
  ensembl protein: ENSP00000348886
  ensembl transcript: ENST00000356493
  gene symbol: STOML2
  variant of: http://identifiers.org/hgnc/14559
canonical: true
consequence: 5' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1367
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 3165
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 393
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 819
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 1850
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13320
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 2890
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8370
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 6.150818058801821e-5
  allele num: 16258
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 63590
  num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: AGCGGAGCGGTC
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum

9-35103131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35103131
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35103131
    reference: chr 9
allele count: 2
allele frequency: 1.723127821621808e-5
allele num: 116068
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165283
  ensembl protein: ENSP00000348886
  ensembl transcript: ENST00000356493
  gene symbol: STOML2
  hgvsc: ENST00000356493.5:c.-40C>T
  variant of: http://identifiers.org/hgnc/14559
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 8145
  bin: 3.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 321
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 181
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2012
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11348
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 864
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8364
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

9-35103133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35103133
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35103133
    reference: chr 9
allele count: 3
allele frequency: 2.5966382190524e-5
allele num: 115534
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165283
  ensembl protein: ENSP00000348886
  ensembl transcript: ENST00000356493
  gene symbol: STOML2
  hgvsc: ENST00000356493.5:c.-42C>T
  variant of: http://identifiers.org/hgnc/14559
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5365
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genotype depth: GenotypeDepth
  all individuals: 11076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 1.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 421
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 11770
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genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 4441
  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 864
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 3
  allele frequency: 2.646903123345686e-4
  allele num: 11334
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 63196
  num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

9-35103133-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35103133
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35103133
    reference: chr 9
allele count: 1
allele frequency: 8.655460730174667e-6
allele num: 115534
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165283
  ensembl protein: ENSP00000348886
  ensembl transcript: ENST00000356493
  gene symbol: STOML2
  hgvsc: ENST00000356493.5:c.-42C>G
  variant of: http://identifiers.org/hgnc/14559
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 11770
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 63196
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8330
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16220
  num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

9-35103136-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35103136
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35103136
    reference: chr 9
allele count: 1
allele frequency: 8.653064049980097e-6
allele num: 115566
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165283
  ensembl protein: ENSP00000348886
  ensembl transcript: ENST00000356493
  gene symbol: STOML2
  hgvsc: ENST00000356493.5:c.-45C>T
  variant of: http://identifiers.org/hgnc/14559
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
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  bin: 1.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8324
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.581427712939242e-5
  allele num: 63234
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11326
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

9-35103136-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35103136
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35103136
    reference: chr 9
allele count: 9
allele frequency: 7.787757644982089e-5
allele num: 115566
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165283
  ensembl protein: ENSP00000348886
  ensembl transcript: ENST00000356493
  gene symbol: STOML2
  hgvsc: ENST00000356493.5:c.-45C>G
  variant of: http://identifiers.org/hgnc/14559
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10696
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
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  allele frequency: 0.0e0
  allele num: 6488
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population: Other
  type: Population
  allele count: 0
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  allele num: 864
  num of homozygotes: 0
population: African
  type: Population
  allele count: 7
  allele frequency: 7.67880649407635e-4
  allele num: 9116
  num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

9-35103137-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35103137
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35103137
    reference: chr 9
allele count: 1
allele frequency: 8.67694016382063e-6
allele num: 115248
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165283
  ensembl protein: ENSP00000348886
  ensembl transcript: ENST00000356493
  gene symbol: STOML2
  hgvsc: ENST00000356493.5:c.-46G>C
  variant of: http://identifiers.org/hgnc/14559
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8300
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population: European (Finnish)
  type: Population
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  allele num: 6478
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16184
  num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/9-35103141-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35103141
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35103141
    reference: chr 9
allele count: 2
allele frequency: 1.731931623339511e-5
allele num: 115478
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165283
  ensembl protein: ENSP00000348886
  ensembl transcript: ENST00000356493
  gene symbol: STOML2
  hgvsc: ENST00000356493.5:c.-50G>T
  variant of: http://identifiers.org/hgnc/14559
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
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genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2815
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2766
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2220
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3201
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2493
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2194
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11870
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5732
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16156
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9194
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11302
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

9-35104580-GCACA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35104580
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35104576
    reference: chr 9
allele count: 1
allele frequency: 7.824726134585289e-5
allele num: 12780
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*634_*637delTGTG
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*634_*637delTGTG
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*634_*637delTGTG
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.*35_*38delTGTG
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*634_*637delTGTG
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*634_*637delTGTG
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*634_*637delTGTG
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*634_*637delTGTG
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2356
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: GCACA
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

9-35104582-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35104582
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35104582
    reference: chr 9
allele count: 1
allele frequency: 7.754342431761787e-5
allele num: 12896
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*636T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*636T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*636T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.*37T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*636T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*636T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*636T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*636T>C
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2235
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1194
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2857
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-35104582-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35104582
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35104582
    reference: chr 9
allele count: 1
allele frequency: 7.754342431761787e-5
allele num: 12896
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*636T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*636T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*636T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.*37T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*636T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*636T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*636T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*636T>A
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2857
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

9-35104593-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35104593
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35104593
    reference: chr 9
allele count: 1
allele frequency: 7.71366862079605e-5
allele num: 12964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*625G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*625G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*625G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*625G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*625G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*625G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.*26G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*625G>A
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2007
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

9-35104609-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35104609
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35104607
    reference: chr 9
allele count: 1
allele frequency: 7.68521364893944e-5
allele num: 13012
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*607_*608delCT
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*607_*608delCT
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*607_*608delCT
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*607_*608delCT
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*607_*608delCT
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.*8_*9delCT
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*607_*608delCT
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*607_*608delCT
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3254
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2762
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: CAG
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

9-35104632-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35104632
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35104632
    reference: chr 9
allele count: 3
allele frequency: 2.390819254064393e-4
allele num: 12548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*586C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*586C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*586C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*586C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*586C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1316C>T
  hgvsp: ENSP00000367816.1:p.Ser439Phe
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*586C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*586C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1194
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3759
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser439Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

9-35104640-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35104640
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35104640
    reference: chr 9
allele count: 10
allele frequency: 8.136696501220504e-4
allele num: 12290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*578C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*578C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*578C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1308C>T
  hgvsp: ENST00000378554.2:c.1308C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*578C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*578C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*578C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*578C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 2927
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro436Pro
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

9-35104652-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35104652
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35104652
    reference: chr 9
allele count: 1
allele frequency: 8.592541673827119e-5
allele num: 11638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*566C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*566C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*566C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*566C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*566C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-9C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*566C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*566C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

9-35104652-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35104652
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35104652
    reference: chr 9
allele count: 16
allele frequency: 1.374806667812339e-3
allele num: 11638
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*566C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*566C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*566C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*566C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-9C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*566C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*566C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*566C>G
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4178
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

9-35105169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105169
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105169
    reference: chr 9
allele count: 1
allele frequency: 8.75902179244622e-6
allele num: 114168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*49C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*49C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*49C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*49C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*49C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*49C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*49C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-526C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10739
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3174
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2474
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2251
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

9-35105173-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105173
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105173
    reference: chr 9
allele count: 1
allele frequency: 8.745080891998251e-6
allele num: 114350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*45T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*45T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*45T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*45T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*45T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*45T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-530T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*45T>C
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13503
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2040
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2839
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3104
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2047
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2128
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

9-35105178-G-GGGCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105178
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105182
    reference: chr 9
allele count: 2
allele frequency: 1.747030048916841e-5
allele num: 114480
alternate allele: GGGCA
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*36_*39dupTGCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-539_1305-536dupTGCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*36_*39dupTGCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*36_*39dupTGCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*36_*39dupTGCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*36_*39dupTGCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*36_*39dupTGCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*36_*39dupTGCC
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17918
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2275
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

9-35105180-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105180
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105180
    reference: chr 9
allele count: 2
allele frequency: 1.745596732242917e-5
allele num: 114574
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*38C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-537C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*38C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1926
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2980
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

9-35105181-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105181
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105181
    reference: chr 9
allele count: 2
allele frequency: 1.747365845987174e-5
allele num: 114458
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*37G>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-538G>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*37G>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*37G>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*37G>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*37G>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*37G>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*37G>C
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18937
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3691
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6585
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

9-35105184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105184
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105184
    reference: chr 9
allele count: 8
allele frequency: 6.963545837540475e-5
allele num: 114884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*34C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*34C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-541C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19952
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3258
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1805
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1961
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

9-35105194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105194
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105194
    reference: chr 9
allele count: 3
allele frequency: 2.600284297749887e-5
allele num: 115372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-551G>A
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7201
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3394
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2677
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2973
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6965
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1550
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

9-35105195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105195
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105195
    reference: chr 9
allele count: 2
allele frequency: 1.732471717399213e-5
allele num: 115442
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*23C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*23C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*23C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*23C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*23C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*23C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-552C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*23C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15761
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3368
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1993
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6958
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

9-35105195-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105195
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105195
    reference: chr 9
allele count: 1
allele frequency: 8.662358586996067e-6
allele num: 115442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*23C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-552C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*23C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*23C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*23C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*23C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*23C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*23C>A
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7427
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2127
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1993
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3260
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

9-35105201-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105201
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105201
    reference: chr 9
allele count: 1
allele frequency: 8.59490494035136e-6
allele num: 116348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.*17C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.*17C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-558C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3108
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2977
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3263
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

9-35105222-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105222
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105222
    reference: chr 9
allele count: 2
allele frequency: 1.687649778917879e-5
allele num: 118508
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1613C>G
  hgvsp: ENSP00000367819.1:p.Pro538Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1613C>G
  hgvsp: ENSP00000474335.1:p.Pro538Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1613C>G
  hgvsp: ENSP00000319897.5:p.Pro538Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.698C>G
  hgvsp: ENSP00000367829.1:p.Pro233Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1613C>G
  hgvsp: ENSP00000474833.1:p.Pro538Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1613C>G
  hgvsp: ENSP00000475120.1:p.Pro538Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1613C>G
  hgvsp: ENSP00000367823.1:p.Pro538Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-579C>G
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18122
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3228
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2933
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1885
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro538Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

9-35105230-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105230
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105230
    reference: chr 9
allele count: 1
allele frequency: 8.387432271484408e-6
allele num: 119226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.690A>G
  hgvsp: ENST00000378566.1:c.690A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-587A>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1605A>G
  hgvsp: ENST00000488109.2:c.1605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1605A>G
  hgvsp: ENST00000378557.1:c.1605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1605A>G
  hgvsp: ENST00000378561.1:c.1605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1605A>G
  hgvsp: ENST00000605244.1:c.1605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1605A>G
  hgvsp: ENST00000603301.1:c.1605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1605A>G
  hgvsp: ENST00000322813.5:c.1605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1464
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser535Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

9-35105237-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105237
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105237
    reference: chr 9
allele count: 1
allele frequency: 8.347106058329577e-6
allele num: 119802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-594G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.683G>A
  hgvsp: ENSP00000367829.1:p.Arg228His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1598G>A
  hgvsp: ENSP00000367819.1:p.Arg533His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1598G>A
  hgvsp: ENSP00000367823.1:p.Arg533His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1598G>A
  hgvsp: ENSP00000475120.1:p.Arg533His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1598G>A
  hgvsp: ENSP00000474335.1:p.Arg533His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1598G>A
  hgvsp: ENSP00000319897.5:p.Arg533His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1598G>A
  hgvsp: ENSP00000474833.1:p.Arg533His
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24160
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19132
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3282
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 1
hgvs: p.Arg533His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

9-35105238-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105238
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105238
    reference: chr 9
allele count: 1
allele frequency: 8.341396683460679e-6
allele num: 119884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1597C>T
  hgvsp: ENSP00000474833.1:p.Arg533Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1597C>T
  hgvsp: ENSP00000319897.5:p.Arg533Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1597C>T
  hgvsp: ENSP00000367823.1:p.Arg533Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1597C>T
  hgvsp: ENSP00000474335.1:p.Arg533Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1597C>T
  hgvsp: ENSP00000367819.1:p.Arg533Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.682C>T
  hgvsp: ENSP00000367829.1:p.Arg228Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1305-595C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1597C>T
  hgvsp: ENSP00000475120.1:p.Arg533Cys
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19189
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg533Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

9-35105245-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105245
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105245
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 120166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.675T>A
  hgvsp: ENSP00000367829.1:p.His225Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1590T>A
  hgvsp: ENSP00000367823.1:p.His530Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+593T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1590T>A
  hgvsp: ENSP00000474335.1:p.His530Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1590T>A
  hgvsp: ENSP00000475120.1:p.His530Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1590T>A
  hgvsp: ENSP00000474833.1:p.His530Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1590T>A
  hgvsp: ENSP00000319897.5:p.His530Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1590T>A
  hgvsp: ENSP00000367819.1:p.His530Gln
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3007
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His530Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

9-35105246-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105246
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105246
    reference: chr 9
allele count: 18
allele frequency: 1.497404498868628e-4
allele num: 120208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1589A>T
  hgvsp: ENSP00000367819.1:p.His530Leu
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1589A>T
  hgvsp: ENSP00000475120.1:p.His530Leu
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1589A>T
  hgvsp: ENSP00000474833.1:p.His530Leu
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1589A>T
  hgvsp: ENSP00000319897.5:p.His530Leu
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.674A>T
  hgvsp: ENSP00000367829.1:p.His225Leu
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1589A>T
  hgvsp: ENSP00000367823.1:p.His530Leu
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1589A>T
  hgvsp: ENSP00000474335.1:p.His530Leu
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+592A>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8301
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24226
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34995
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His530Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

9-35105256-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105256
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105256
    reference: chr 9
allele count: 1
allele frequency: 8.303854649328218e-6
allele num: 120426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1579G>A
  hgvsp: ENSP00000367819.1:p.Glu527Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1579G>A
  hgvsp: ENSP00000475120.1:p.Glu527Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1579G>A
  hgvsp: ENSP00000474335.1:p.Glu527Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1579G>A
  hgvsp: ENSP00000367823.1:p.Glu527Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.664G>A
  hgvsp: ENSP00000367829.1:p.Glu222Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+582G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1579G>A
  hgvsp: ENSP00000474833.1:p.Glu527Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1579G>A
  hgvsp: ENSP00000319897.5:p.Glu527Lys
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19965
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3377
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3044
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu527Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

9-35105257-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105257
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105257
    reference: chr 9
allele count: 13660
allele frequency: 1.134155859251756e-1
allele num: 120442
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.663C>T
  hgvsp: ENST00000378566.1:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1578C>T
  hgvsp: ENST00000378557.1:c.1578C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1578C>T
  hgvsp: ENST00000322813.5:c.1578C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1578C>T
  hgvsp: ENST00000488109.2:c.1578C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1578C>T
  hgvsp: ENST00000378561.1:c.1578C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1578C>T
  hgvsp: ENST00000603301.1:c.1578C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+581C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1578C>T
  hgvsp: ENST00000605244.1:c.1578C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 19670
  bin: 2.25e1
  variant carriers: 841
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 1.75e1
  variant carriers: 338
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 3.25e1
  variant carriers: 1885
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 4.75e1
  variant carriers: 1195
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18232
  bin: 2.75e1
  variant carriers: 1523
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 1.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 165
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 3.75e1
  variant carriers: 1898
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 4.25e1
  variant carriers: 1572
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 376
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.25e1
  variant carriers: 822
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.75e1
  variant carriers: 600
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.75e1
  variant carriers: 447
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 2.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 29963
  bin: 6.25e1
  variant carriers: 39
hgvs: p.Thr526Thr
num of homozygotes: 1359
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

9-35105261-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105261
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105261
    reference: chr 9
allele count: 1
allele frequency: 8.287888080359362e-6
allele num: 120658
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.659T>C
  hgvsp: ENSP00000367829.1:p.Val220Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1574T>C
  hgvsp: ENSP00000474335.1:p.Val525Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1574T>C
  hgvsp: ENSP00000475120.1:p.Val525Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1574T>C
  hgvsp: ENSP00000367819.1:p.Val525Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1574T>C
  hgvsp: ENSP00000474833.1:p.Val525Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+577T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1574T>C
  hgvsp: ENSP00000367823.1:p.Val525Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1574T>C
  hgvsp: ENSP00000319897.5:p.Val525Ala
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22193
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2926
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val525Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

9-35105262-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105262
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105262
    reference: chr 9
allele count: 1
allele frequency: 8.287888080359362e-6
allele num: 120658
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1573G>A
  hgvsp: ENSP00000319897.5:p.Val525Met
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1573G>A
  hgvsp: ENSP00000474833.1:p.Val525Met
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1573G>A
  hgvsp: ENSP00000367823.1:p.Val525Met
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.658G>A
  hgvsp: ENSP00000367829.1:p.Val220Met
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1573G>A
  hgvsp: ENSP00000367819.1:p.Val525Met
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1573G>A
  hgvsp: ENSP00000475120.1:p.Val525Met
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1573G>A
  hgvsp: ENSP00000474335.1:p.Val525Met
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+576G>A
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9695
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val525Met
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: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-35105270-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105270
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105270
    reference: chr 9
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1565T>G
  hgvsp: ENSP00000474335.1:p.Leu522Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1565T>G
  hgvsp: ENSP00000319897.5:p.Leu522Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.650T>G
  hgvsp: ENSP00000367829.1:p.Leu217Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1565T>G
  hgvsp: ENSP00000474833.1:p.Leu522Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1565T>G
  hgvsp: ENSP00000367819.1:p.Leu522Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1565T>G
  hgvsp: ENSP00000367823.1:p.Leu522Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1565T>G
  hgvsp: ENSP00000475120.1:p.Leu522Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+568T>G
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20394
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1959
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu522Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD

9-35105274-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105274
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105274
    reference: chr 9
allele count: 6
allele frequency: 4.969602597445624e-5
allele num: 120734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.646G>A
  hgvsp: ENSP00000367829.1:p.Glu216Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1561G>A
  hgvsp: ENSP00000475120.1:p.Glu521Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1561G>A
  hgvsp: ENSP00000474833.1:p.Glu521Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1561G>A
  hgvsp: ENSP00000474335.1:p.Glu521Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1561G>A
  hgvsp: ENSP00000367823.1:p.Glu521Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1561G>A
  hgvsp: ENSP00000367819.1:p.Glu521Lys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+564G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1561G>A
  hgvsp: ENSP00000319897.5:p.Glu521Lys
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2887
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8285
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu521Lys
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

9-35105275-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105275
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105275
    reference: chr 9
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+563C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1560C>T
  hgvsp: ENST00000322813.5:c.1560C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1560C>T
  hgvsp: ENST00000378561.1:c.1560C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1560C>T
  hgvsp: ENST00000378557.1:c.1560C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.645C>T
  hgvsp: ENST00000378566.1:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1560C>T
  hgvsp: ENST00000603301.1:c.1560C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1560C>T
  hgvsp: ENST00000605244.1:c.1560C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1560C>T
  hgvsp: ENST00000488109.2:c.1560C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37079
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3027
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr520Tyr
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

9-35105276-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105276
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105276
    reference: chr 9
allele count: 2
allele frequency: 1.65582103886212e-5
allele num: 120786
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1559A>G
  hgvsp: ENSP00000475120.1:p.Tyr520Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1559A>G
  hgvsp: ENSP00000474335.1:p.Tyr520Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1559A>G
  hgvsp: ENSP00000367819.1:p.Tyr520Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1559A>G
  hgvsp: ENSP00000319897.5:p.Tyr520Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1559A>G
  hgvsp: ENSP00000474833.1:p.Tyr520Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1559A>G
  hgvsp: ENSP00000367823.1:p.Tyr520Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.644A>G
  hgvsp: ENSP00000367829.1:p.Tyr215Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+562A>G
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9667
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37234
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8333
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr520Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

9-35105280-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105280
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105280
    reference: chr 9
allele count: 1
allele frequency: 8.277460475126231e-6
allele num: 120810
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1555C>T
  hgvsp: ENSP00000367823.1:p.Pro519Ser
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.640C>T
  hgvsp: ENSP00000367829.1:p.Pro214Ser
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1555C>T
  hgvsp: ENSP00000367819.1:p.Pro519Ser
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+558C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1555C>T
  hgvsp: ENSP00000474335.1:p.Pro519Ser
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1555C>T
  hgvsp: ENSP00000474833.1:p.Pro519Ser
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1555C>T
  hgvsp: ENSP00000319897.5:p.Pro519Ser
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1555C>T
  hgvsp: ENSP00000475120.1:p.Pro519Ser
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3025
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2890
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2396
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro519Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

9-35105286-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105286
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105286
    reference: chr 9
allele count: 1
allele frequency: 8.276501357346223e-6
allele num: 120824
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1549G>C
  hgvsp: ENSP00000319897.5:p.Gly517Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1549G>C
  hgvsp: ENSP00000474335.1:p.Gly517Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1549G>C
  hgvsp: ENSP00000367823.1:p.Gly517Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+552G>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1549G>C
  hgvsp: ENSP00000367819.1:p.Gly517Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.634G>C
  hgvsp: ENSP00000367829.1:p.Gly212Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1549G>C
  hgvsp: ENSP00000474833.1:p.Gly517Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1549G>C
  hgvsp: ENSP00000475120.1:p.Gly517Arg
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22681
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2859
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly517Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

9-35105289-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105289
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105289
    reference: chr 9
allele count: 1
allele frequency: 8.274036074797286e-6
allele num: 120860
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1546A>G
  hgvsp: ENSP00000367823.1:p.Thr516Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1546A>G
  hgvsp: ENSP00000474335.1:p.Thr516Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1546A>G
  hgvsp: ENSP00000319897.5:p.Thr516Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1546A>G
  hgvsp: ENSP00000475120.1:p.Thr516Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1546A>G
  hgvsp: ENSP00000367819.1:p.Thr516Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1546A>G
  hgvsp: ENSP00000474833.1:p.Thr516Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.631A>G
  hgvsp: ENSP00000367829.1:p.Thr211Ala
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+549A>G
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22796
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr516Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

9-35105302-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105302
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105302
    reference: chr 9
allele count: 1
allele frequency: 8.27417299640901e-6
allele num: 120858
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1533C>A
  hgvsp: ENSP00000367823.1:p.Ser511Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1533C>A
  hgvsp: ENSP00000474335.1:p.Ser511Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+536C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1533C>A
  hgvsp: ENSP00000474833.1:p.Ser511Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.618C>A
  hgvsp: ENSP00000367829.1:p.Ser206Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1533C>A
  hgvsp: ENSP00000367819.1:p.Ser511Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1533C>A
  hgvsp: ENSP00000475120.1:p.Ser511Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1533C>A
  hgvsp: ENSP00000319897.5:p.Ser511Arg
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23344
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2387
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser511Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP

9-35105304-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105304
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105304
    reference: chr 9
allele count: 1
allele frequency: 8.272940865018697e-6
allele num: 120876
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1531A>T
  hgvsp: ENSP00000319897.5:p.Ser511Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1531A>T
  hgvsp: ENSP00000367823.1:p.Ser511Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1531A>T
  hgvsp: ENSP00000474833.1:p.Ser511Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+534A>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1531A>T
  hgvsp: ENSP00000474335.1:p.Ser511Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.616A>T
  hgvsp: ENSP00000367829.1:p.Ser206Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1531A>T
  hgvsp: ENSP00000367819.1:p.Ser511Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1531A>T
  hgvsp: ENSP00000475120.1:p.Ser511Cys
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2812
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser511Cys
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-35105307-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105307
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105307
    reference: chr 9
allele count: 3
allele frequency: 2.482046530098951e-5
allele num: 120868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1528C>T
  hgvsp: ENSP00000319897.5:p.Arg510Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.613C>T
  hgvsp: ENSP00000367829.1:p.Arg205Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+531C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1528C>T
  hgvsp: ENSP00000474335.1:p.Arg510Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1528C>T
  hgvsp: ENSP00000475120.1:p.Arg510Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1528C>T
  hgvsp: ENSP00000474833.1:p.Arg510Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1528C>T
  hgvsp: ENSP00000367819.1:p.Arg510Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1528C>T
  hgvsp: ENSP00000367823.1:p.Arg510Trp
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9782
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1922
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8280
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg510Trp
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

9-35105309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105309
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105309
    reference: chr 9
allele count: 5
allele frequency: 4.137291894217721e-5
allele num: 120852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1526G>A
  hgvsp: ENSP00000319897.5:p.Arg509His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.611G>A
  hgvsp: ENSP00000367829.1:p.Arg204His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+529G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1526G>A
  hgvsp: ENSP00000474335.1:p.Arg509His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1526G>A
  hgvsp: ENSP00000367823.1:p.Arg509His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1526G>A
  hgvsp: ENSP00000474833.1:p.Arg509His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1526G>A
  hgvsp: ENSP00000475120.1:p.Arg509His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1526G>A
  hgvsp: ENSP00000367819.1:p.Arg509His
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9808
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8251
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg509His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

9-35105311-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105311
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105311
    reference: chr 9
allele count: 8
allele frequency: 6.617695718350871e-5
allele num: 120888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.609C>T
  hgvsp: ENST00000378566.1:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1524C>T
  hgvsp: ENST00000378561.1:c.1524C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1524C>T
  hgvsp: ENST00000488109.2:c.1524C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1524C>T
  hgvsp: ENST00000603301.1:c.1524C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1524C>T
  hgvsp: ENST00000605244.1:c.1524C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+527C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1524C>T
  hgvsp: ENST00000378557.1:c.1524C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1524C>T
  hgvsp: ENST00000322813.5:c.1524C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser508Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

9-35105325-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105325
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105325
    reference: chr 9
allele count: 14
allele frequency: 1.158614297300429e-4
allele num: 120834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1510C>T
  hgvsp: ENSP00000367819.1:p.Arg504Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1510C>T
  hgvsp: ENSP00000474833.1:p.Arg504Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.595C>T
  hgvsp: ENSP00000367829.1:p.Arg199Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+513C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1510C>T
  hgvsp: ENSP00000475120.1:p.Arg504Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1510C>T
  hgvsp: ENSP00000367823.1:p.Arg504Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1510C>T
  hgvsp: ENSP00000319897.5:p.Arg504Cys
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1510C>T
  hgvsp: ENSP00000474335.1:p.Arg504Cys
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23850
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg504Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS

9-35105327-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105327
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105327
    reference: chr 9
allele count: 1
allele frequency: 8.277597510098669e-6
allele num: 120808
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1508T>C
  hgvsp: ENSP00000367819.1:p.Ile503Thr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1508T>C
  hgvsp: ENSP00000474335.1:p.Ile503Thr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1508T>C
  hgvsp: ENSP00000474833.1:p.Ile503Thr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.593T>C
  hgvsp: ENSP00000367829.1:p.Ile198Thr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1508T>C
  hgvsp: ENSP00000367823.1:p.Ile503Thr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+511T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1508T>C
  hgvsp: ENSP00000475120.1:p.Ile503Thr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1508T>C
  hgvsp: ENSP00000319897.5:p.Ile503Thr
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8246
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ile503Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

9-35105329-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105329
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105329
    reference: chr 9
allele count: 2
allele frequency: 1.655985559805918e-5
allele num: 120774
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1506T>C
  hgvsp: ENST00000605244.1:c.1506T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1506T>C
  hgvsp: ENST00000322813.5:c.1506T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.591T>C
  hgvsp: ENST00000378566.1:c.591T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+509T>C
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1506T>C
  hgvsp: ENST00000603301.1:c.1506T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1506T>C
  hgvsp: ENST00000378557.1:c.1506T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1506T>C
  hgvsp: ENST00000378561.1:c.1506T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1506T>C
  hgvsp: ENST00000488109.2:c.1506T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39321
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Asp502Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/9-35105331-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105331
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105331
    reference: chr 9
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1504G>T
  hgvsp: ENSP00000474833.1:p.Asp502Tyr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1504G>T
  hgvsp: ENSP00000367823.1:p.Asp502Tyr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+507G>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1504G>T
  hgvsp: ENSP00000319897.5:p.Asp502Tyr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.589G>T
  hgvsp: ENSP00000367829.1:p.Asp197Tyr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1504G>T
  hgvsp: ENSP00000475120.1:p.Asp502Tyr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1504G>T
  hgvsp: ENSP00000474335.1:p.Asp502Tyr
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1504G>T
  hgvsp: ENSP00000367819.1:p.Asp502Tyr
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp502Tyr
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

9-35105336-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105336
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105336
    reference: chr 9
allele count: 2
allele frequency: 1.657660047077545e-5
allele num: 120652
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.584A>G
  hgvsp: ENSP00000367829.1:p.His195Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1499A>G
  hgvsp: ENSP00000319897.5:p.His500Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1499A>G
  hgvsp: ENSP00000474335.1:p.His500Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+502A>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1499A>G
  hgvsp: ENSP00000474833.1:p.His500Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1499A>G
  hgvsp: ENSP00000367819.1:p.His500Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1499A>G
  hgvsp: ENSP00000475120.1:p.His500Arg
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1499A>G
  hgvsp: ENSP00000367823.1:p.His500Arg
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20197
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1904
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39399
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2782
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His500Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

9-35105348-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105348
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105348
    reference: chr 9
allele count: 2
allele frequency: 1.66858554003771e-5
allele num: 119862
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.572G>A
  hgvsp: ENSP00000367829.1:p.Arg191His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+490G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1487G>A
  hgvsp: ENSP00000319897.5:p.Arg496His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1487G>A
  hgvsp: ENSP00000367819.1:p.Arg496His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1487G>A
  hgvsp: ENSP00000367823.1:p.Arg496His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1487G>A
  hgvsp: ENSP00000474335.1:p.Arg496His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1487G>A
  hgvsp: ENSP00000474833.1:p.Arg496His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1487G>A
  hgvsp: ENSP00000475120.1:p.Arg496His
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2710
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg496His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ

9-35105350-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105350
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105350
    reference: chr 9
allele count: 1
allele frequency: 8.34599142032082e-6
allele num: 119818
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1485C>T
  hgvsp: ENST00000378561.1:c.1485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1485C>T
  hgvsp: ENST00000378557.1:c.1485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.570C>T
  hgvsp: ENST00000378566.1:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1485C>T
  hgvsp: ENST00000605244.1:c.1485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1485C>T
  hgvsp: ENST00000488109.2:c.1485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1485C>T
  hgvsp: ENST00000322813.5:c.1485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1485C>T
  hgvsp: ENST00000603301.1:c.1485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+488C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly495Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD

9-35105357-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105357
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105357
    reference: chr 9
allele count: 1
allele frequency: 8.403220113947665e-6
allele num: 119002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1478G>A
  hgvsp: ENSP00000319897.5:p.Arg493His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1478G>A
  hgvsp: ENSP00000367823.1:p.Arg493His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1478G>A
  hgvsp: ENSP00000475120.1:p.Arg493His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1478G>A
  hgvsp: ENSP00000367819.1:p.Arg493His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.563G>A
  hgvsp: ENSP00000367829.1:p.Arg188His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+481G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1478G>A
  hgvsp: ENSP00000474335.1:p.Arg493His
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1478G>A
  hgvsp: ENSP00000474833.1:p.Arg493His
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1886
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37508
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg493His
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

9-35105366-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105366
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105366
    reference: chr 9
allele count: 4
allele frequency: 3.383293297695977e-5
allele num: 118228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.554G>A
  hgvsp: ENSP00000367829.1:p.Arg185Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1469G>A
  hgvsp: ENSP00000475120.1:p.Arg490Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1469G>A
  hgvsp: ENSP00000367819.1:p.Arg490Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1469G>A
  hgvsp: ENSP00000367823.1:p.Arg490Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1469G>A
  hgvsp: ENSP00000474833.1:p.Arg490Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1469G>A
  hgvsp: ENSP00000474335.1:p.Arg490Gln
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+472G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1469G>A
  hgvsp: ENSP00000319897.5:p.Arg490Gln
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22872
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9292
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18526
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2808
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36698
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg490Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

9-35105367-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105367
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105367
    reference: chr 9
allele count: 1
allele frequency: 8.489540885628905e-6
allele num: 117792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1468C>T
  hgvsp: ENSP00000367819.1:p.Arg490Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+471C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1468C>T
  hgvsp: ENSP00000474335.1:p.Arg490Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1468C>T
  hgvsp: ENSP00000474833.1:p.Arg490Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1468C>T
  hgvsp: ENSP00000319897.5:p.Arg490Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.553C>T
  hgvsp: ENSP00000367829.1:p.Arg185Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1468C>T
  hgvsp: ENSP00000367823.1:p.Arg490Trp
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1468C>T
  hgvsp: ENSP00000475120.1:p.Arg490Trp
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18165
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg490Trp
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

9-35105373-TGGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105373
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105370
    reference: chr 9
allele count: 1
allele frequency: 8.510493438409559e-6
allele num: 117502
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-5_1464-3delTCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-5_1464-3delTCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-5_1464-3delTCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-5_1464-3delTCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-5_549-3delTCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-5_1464-3delTCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+462_1304+464delTCC
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-5_1464-3delTCC
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1464-5_1464-3delTCC
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: TGGA
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

9-35105375-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105375
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105375
    reference: chr 9
allele count: 1
allele frequency: 8.522678848415634e-6
allele num: 117334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-4C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-4C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+463C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-4C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-4C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-4C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-4C>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-4C>A
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17774
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35498
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1464-4C>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

9-35105377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105377
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105377
    reference: chr 9
allele count: 1
allele frequency: 8.540293102859289e-6
allele num: 117092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-6C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-6C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-6C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-6C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-6C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+461C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-6C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-6C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22088
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34845
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
hgvs: c.1464-6C>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

9-35105385-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105385
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105385
    reference: chr 9
allele count: 1
allele frequency: 8.589294303580018e-6
allele num: 116424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-14T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-14T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-14T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-14T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-14T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-14T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+453T>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-14T>A
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33867
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

9-35105395-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105395
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105395
    reference: chr 9
allele count: 1
allele frequency: 8.683721495684191e-6
allele num: 115158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+443G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-24G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-24G>A
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5743
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15125
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5426
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1779
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

9-35105396-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105396
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105396
    reference: chr 9
allele count: 3
allele frequency: 2.605297438124186e-5
allele num: 115150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+442C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-25C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-25C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-25C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-25C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-25C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-25C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-25C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15104
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31005
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7055
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS

9-35105396-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105396
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105396
    reference: chr 9
allele count: 6
allele frequency: 5.210594876248371e-5
allele num: 115150
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-25C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-25C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-25C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-25C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-25C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-25C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-25C>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+442C>G
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2474
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5526
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

9-35105396-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105396
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105397
    reference: chr 9
allele count: 1
allele frequency: 8.684324793747287e-6
allele num: 115150
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-26dupA
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-26dupA
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-26dupA
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-26dupA
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+441dupA
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-26dupA
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-26dupA
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-26dupA
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5526
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2693
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

9-35105404-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105404
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105404
    reference: chr 9
allele count: 1
allele frequency: 8.7631666579035e-6
allele num: 114114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+434G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-33G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-33G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-33G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-33G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-33G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-33G>A
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-33G>A
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1806
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5579
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6810
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2355
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

9-35105408-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105408
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105408
    reference: chr 9
allele count: 2
allele frequency: 1.762766838830228e-5
allele num: 113458
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-37C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-37C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-37C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-37C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-37C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+430C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-37C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-37C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16988
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23528
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2386
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1302
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6452
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

9-35105410-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105410
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105410
    reference: chr 9
allele count: 1
allele frequency: 8.863990923273295e-6
allele num: 112816
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-39A>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-39A>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-39A>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-39A>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-39A>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-39A>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-39A>G
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+428A>G
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12176
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2351
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5181
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5895
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3799
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

9-35105411-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35105411
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 35105411
    reference: chr 9
allele count: 3
allele frequency: 2.662076064386746e-5
allele num: 112694
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474335
  ensembl transcript: ENST00000603301
  gene symbol: FAM214B
  hgvsc: ENST00000603301.1:c.1464-40C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367823
  ensembl transcript: ENST00000378561
  gene symbol: FAM214B
  hgvsc: ENST00000378561.1:c.1464-40C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000474833
  ensembl transcript: ENST00000605244
  gene symbol: FAM214B
  hgvsc: ENST00000605244.1:c.1464-40C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367819
  ensembl transcript: ENST00000378557
  gene symbol: FAM214B
  hgvsc: ENST00000378557.1:c.1464-40C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000475120
  ensembl transcript: ENST00000488109
  gene symbol: FAM214B
  hgvsc: ENST00000488109.2:c.1464-40C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367816
  ensembl transcript: ENST00000378554
  gene symbol: FAM214B
  hgvsc: ENST00000378554.2:c.1304+427C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000367829
  ensembl transcript: ENST00000378566
  gene symbol: FAM214B
  hgvsc: ENST00000378566.1:c.549-40C>T
  variant of: http://identifiers.org/hgnc/25666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005238
  ensembl protein: ENSP00000319897
  ensembl transcript: ENST00000322813
  gene symbol: FAM214B
  hgvsc: ENST00000322813.5:c.1464-40C>T
  variant of: http://identifiers.org/hgnc/25666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: G

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.57400994774287e-5
allele num: 63532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.413e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

DP
type: SiteQuality
SIO_000300: 1.910214e6

QD
type: SiteQuality
SIO_000300: 1.347e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.021e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.32e0

QD
type: SiteQuality
SIO_000300: 1.87e0

VQSLOD
type: SiteQuality
SIO_000300: -4.417e-1

MQ
type: SiteQuality
SIO_000300: 5.427e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

DP
type: SiteQuality
SIO_000300: 1.90932e6

FS
type: SiteQuality
SIO_000300: 2.442e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.573910853689247e-5
allele num: 63536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.08695652173913e-4
allele num: 9200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.905258e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

FS
type: SiteQuality
SIO_000300: 1.553e0

VQSLOD
type: SiteQuality
SIO_000300: -6.187e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.225e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.201e0

QD
type: SiteQuality
SIO_000300: 8.130000000000001e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

DP
type: SiteQuality
SIO_000300: 1.889177e6

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.366e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.372e0

VQSLOD
type: SiteQuality
SIO_000300: 8.95e-1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9104
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.823010411152286e-5
allele num: 11334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.889177e6

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

QD
type: SiteQuality
SIO_000300: 1.278e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.372e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-2

FS
type: SiteQuality
SIO_000300: 3.366e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9116
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

QD
type: SiteQuality
SIO_000300: 1.396e1

FS
type: SiteQuality
SIO_000300: 3.168e0

MQRankSum
type: SiteQuality
SIO_000300: -4.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.83e-1

DP
type: SiteQuality
SIO_000300: 1.880278e6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.765848490199541e-4
allele num: 11326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63234
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.168e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

DP
type: SiteQuality
SIO_000300: 1.880278e6

MQRankSum
type: SiteQuality
SIO_000300: -4.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

QD
type: SiteQuality
SIO_000300: 1.396e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.103022281050077e-4
allele num: 9066
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63052
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.979e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.662e1

DP
type: SiteQuality
SIO_000300: 1.875184e6

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.581627811343435e-5
allele num: 63226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.21036068748487e-4
allele num: 8262
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.639e1

MQRankSum
type: SiteQuality
SIO_000300: 9.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

FS
type: SiteQuality
SIO_000300: 3.848e0

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.78e-1

DP
type: SiteQuality
SIO_000300: 1.867806e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

GenotypeQuality
all individuals: 2802
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1576
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.066115702479339e-3
allele num: 484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 936
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4766
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.149e0

MQ
type: SiteQuality
SIO_000300: 5.868e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.74e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.55e-1

QD
type: SiteQuality
SIO_000300: 1.316e1

VQSLOD
type: SiteQuality
SIO_000300: 3.91e0

DP
type: SiteQuality
SIO_000300: 2.04782e5

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.062706270627063e-4
allele num: 4848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 940
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.72e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.128e1

DP
type: SiteQuality
SIO_000300: 2.05412e5

VQSLOD
type: SiteQuality
SIO_000300: 2.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.29e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 629
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4848
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.063829787234043e-3
allele num: 940
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.72e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.05412e5

QD
type: SiteQuality
SIO_000300: 1.128e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.29e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

GenotypeQuality
all individuals: 2413
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 2.041649652919559e-4
allele num: 4898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 938
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

QD
type: SiteQuality
SIO_000300: 1.124e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

DP
type: SiteQuality
SIO_000300: 2.12479e5

FS
type: SiteQuality
SIO_000300: 3.334e0

VQSLOD
type: SiteQuality
SIO_000300: 3.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.02e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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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
all individuals: 132
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4666
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.051702913418137e-4
allele num: 4874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.59e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

DP
type: SiteQuality
SIO_000300: 2.1809e5

MQ
type: SiteQuality
SIO_000300: 5.833e1

QD
type: SiteQuality
SIO_000300: 1.486e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 46
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 273
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GenotypeQuality
all individuals: 119
bin: 7.25e1
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GenotypeQuality
all individuals: 299
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.239740820734341e-3
allele num: 926
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4558
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: -4.051e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.78e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.12416e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 94
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GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 916
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 7.936507936507936e-3
allele num: 252
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.786511835640911e-3
allele num: 4478
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.69e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
SIO_000300: 1.444e1

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

FS
type: SiteQuality
SIO_000300: 5.17e-1

DP
type: SiteQuality
SIO_000300: 2.08438e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.428e0

MQRankSum
type: SiteQuality
SIO_000300: -3.81e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.561475409836066e-4
allele num: 3904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4320
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 1.99617e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.83e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.032e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 14

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3904
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

African
type: Population
allele count: 16
allele frequency: 1.762114537444934e-2
allele num: 908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4320
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: 4.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.83e-2

QD
type: SiteQuality
SIO_000300: 1.032e1

DP
type: SiteQuality
SIO_000300: 1.99617e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.939746111210442e-5
allele num: 11186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.1e0

FS
type: SiteQuality
SIO_000300: 6.429e0

DP
type: SiteQuality
SIO_000300: 1.426052e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.29e-1

QD
type: SiteQuality
SIO_000300: 1.442e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2496
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55077228459773e-5
allele num: 64484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10052
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12890
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

FS
type: SiteQuality
SIO_000300: 1.372e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.039e0

VQSLOD
type: SiteQuality
SIO_000300: -3.125e0

QD
type: SiteQuality
SIO_000300: 4.25e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

MQRankSum
type: SiteQuality
SIO_000300: -2.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e-1

DP
type: SiteQuality
SIO_000300: 1.437159e6

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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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11232
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64542
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.54273372415921e-4
allele num: 12964
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.454548e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.926e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.65e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

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

South Asian
type: Population
allele count: 2
allele frequency: 1.537751806858373e-4
allele num: 13006
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64570
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
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MQRankSum
type: SiteQuality
SIO_000300: -4.53e-1

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e0

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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11230
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Finnish)
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allele count: 0
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Other
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allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64528
num of homozygotes: 0

African
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allele count: 0
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South Asian
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allele count: 2
allele frequency: 1.545595054095827e-4
allele num: 12940
num of homozygotes: 0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6730
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10080
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South Asian
type: Population
allele count: 8
allele frequency: 6.088280060882801e-4
allele num: 13140
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.674e0

QD
type: SiteQuality
SIO_000300: 1.312e1

FS
type: SiteQuality
SIO_000300: 3.902e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

DP
type: SiteQuality
SIO_000300: 1.476828e6

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

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: 3

GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542638528939899e-5
allele num: 64824
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.333722287047841e-4
allele num: 8570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.83e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.405e0

QD
type: SiteQuality
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DP
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MQ
type: SiteQuality
SIO_000300: 5.904e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.11e-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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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11270
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.924573243350536e-5
allele num: 10076
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64820
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 7.405213270142181e-5
allele num: 13504
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.43e0

MQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

DP
type: SiteQuality
SIO_000300: 1.524486e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.944e0

FS
type: SiteQuality
SIO_000300: 1.2612e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.04e-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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.54273372415921e-5
allele num: 64820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10076
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 6.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

FS
type: SiteQuality
SIO_000300: 1.2612e1

VQSLOD
type: SiteQuality
SIO_000300: -1.944e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.72e-1

DP
type: SiteQuality
SIO_000300: 1.524486e6

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
all individuals: 849
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535532215465881e-5
allele num: 65124
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13928
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.429e0

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 8.2e-2

MQ
type: SiteQuality
SIO_000300: 5.98e1

MQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

FS
type: SiteQuality
SIO_000300: 1.2292e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.74e-1

DP
type: SiteQuality
SIO_000300: 1.546702e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15178
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.03951367781155e-5
allele num: 65800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.596455e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514142087093453e-5
allele num: 66044
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
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ClippingRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
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ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66190
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 9.746588693957115e-5
allele num: 10260
num of homozygotes: 0

South Asian
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FS
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQRankSum
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DP
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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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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South Asian
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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 frequency: 1.510117789187557e-5
allele num: 66220
num of homozygotes: 0

European (Finnish)
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Latino
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allele frequency: 0.0e0
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African
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Other
type: Population
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allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

FS
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele frequency: 0.0e0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16122
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.566e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.29e-1

DP
type: SiteQuality
SIO_000300: 1.62885e6

QD
type: SiteQuality
SIO_000300: 4.16e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 18

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1040
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

Latino
type: Population
allele count: 18
allele frequency: 1.568490763332171e-3
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16144
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.07e-1

QD
type: SiteQuality
SIO_000300: 1.324e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

MQRankSum
type: SiteQuality
SIO_000300: 5.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.103e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.629769e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

GenotypeQuality
all individuals: 17
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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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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66388
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.159152500615915e-5
allele num: 16236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.656e-1

QD
type: SiteQuality
SIO_000300: 1.51e1

FS
type: SiteQuality
SIO_000300: 6.763e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.639994e6

MQ
type: SiteQuality
SIO_000300: 5.907e1

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 45

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 79

GenotypeQuality
all individuals: 474
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variant carriers: 27

GenotypeQuality
all individuals: 13483
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variant carriers: 11762

Other
type: Population
allele count: 95
allele frequency: 1.060267857142857e-1
allele num: 896
num of homozygotes: 4

Latino
type: Population
allele count: 1805
allele frequency: 1.573121840683284e-1
allele num: 11474
num of homozygotes: 140

South Asian
type: Population
allele count: 2710
allele frequency: 1.662168792934249e-1
allele num: 16304
num of homozygotes: 268

European (Non-Finnish)
type: Population
allele count: 3220
allele frequency: 4.850274145929987e-2
allele num: 66388
num of homozygotes: 95

East Asian
type: Population
allele count: 3296
allele frequency: 3.837019790454017e-1
allele num: 8590
num of homozygotes: 622

African
type: Population
allele count: 2055
allele frequency: 1.989736638264911e-1
allele num: 10328
num of homozygotes: 210

European (Finnish)
type: Population
allele count: 479
allele frequency: 7.41256576911173e-2
allele num: 6462
num of homozygotes: 20

VQSLOD
type: SiteQuality
SIO_000300: 7.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.74e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 1.576e1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

DP
type: SiteQuality
SIO_000300: 1.812375e6

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
all individuals: 966
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GenotypeQuality
all individuals: 221
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504392827055001e-5
allele num: 66472
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
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: 16318
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e-1

DP
type: SiteQuality
SIO_000300: 1.636912e6

QD
type: SiteQuality
SIO_000300: 1.467e1

VQSLOD
type: SiteQuality
SIO_000300: 5.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.37e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

MQRankSum
type: SiteQuality
SIO_000300: -1.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e-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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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: 10344
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16326
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504392827055001e-5
allele num: 66472
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

FS
type: SiteQuality
SIO_000300: 1.607e0

DP
type: SiteQuality
SIO_000300: 1.637442e6

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -5.79e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.7e-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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South Asian
type: Population
allele count: 1
allele frequency: 6.118453255017132e-5
allele num: 16344
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66506
num of homozygotes: 0

Other
type: Population
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

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

VQSLOD
type: SiteQuality
SIO_000300: 2.97e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele count: 0
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allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
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European (Non-Finnish)
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allele count: 4
allele frequency: 6.013952369497234e-5
allele num: 66512
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 2
allele frequency: 1.223091976516634e-4
allele num: 16352
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 359
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 6.112469437652811e-5
allele num: 16360
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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VQSLOD
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MQRankSum
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QD
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DP
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ClippingRankSum
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FS
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3031
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005801196308876e-5
allele num: 66538
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 3.462e1

MQ
type: SiteQuality
SIO_000300: 5.929e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

FS
type: SiteQuality
SIO_000300: 3.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.185e0

VQSLOD
type: SiteQuality
SIO_000300: -1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.64097e6

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

GenotypeQuality
all individuals: 404
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.25e1
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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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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 8.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66528
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.682062858135092e-5
allele num: 11518
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-1

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

DP
type: SiteQuality
SIO_000300: 1.642137e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.207e0

FS
type: SiteQuality
SIO_000300: 1.226e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e-1

GenotypeQuality
all individuals: 258
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3006
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.107243190423842e-5
allele num: 16374
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.64399e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.442e0

QD
type: SiteQuality
SIO_000300: 5.72e0

FS
type: SiteQuality
SIO_000300: 1.596e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.249e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.28e-1

GenotypeQuality
all individuals: 341
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 224
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GenotypeQuality
all individuals: 3002
bin: 7.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.10798924993892e-5
allele num: 16372
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.644521e6

VQSLOD
type: SiteQuality
SIO_000300: -7.865e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

FS
type: SiteQuality
SIO_000300: 1.657e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e-1

QD
type: SiteQuality
SIO_000300: 5.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 235
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 8.75e1
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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2816
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502268425322237e-5
allele num: 66566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.425e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.19e-1

FS
type: SiteQuality
SIO_000300: 6.329e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.352e1

MQRankSum
type: SiteQuality
SIO_000300: -6.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.650108e6

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 544
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2387
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502133028901039e-5
allele num: 66572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

MQ
type: SiteQuality
SIO_000300: 5.725e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.321e0

QD
type: SiteQuality
SIO_000300: 1.152e1

VQSLOD
type: SiteQuality
SIO_000300: -2.653e0

DP
type: SiteQuality
SIO_000300: 1.651076e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.637e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

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

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

African
type: Population
allele count: 3
allele frequency: 2.896871378910776e-4
allele num: 10356
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.090000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.714e1

DP
type: SiteQuality
SIO_000300: 1.652998e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

FS
type: SiteQuality
SIO_000300: 6.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

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

GenotypeQuality
all individuals: 2941
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 280
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variant carriers: 0

GenotypeQuality
all individuals: 180
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GenotypeQuality
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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: 2389
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
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: 3
allele frequency: 4.507888805409467e-5
allele num: 66550
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.931247585940518e-4
allele num: 10356
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.654659e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.016e0

FS
type: SiteQuality
SIO_000300: 3.227e0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

QD
type: SiteQuality
SIO_000300: 1.188e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
bin: 1.75e1
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2947
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
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: 8
allele frequency: 9.252833680314596e-4
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66568
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.65487e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.75e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 6.29e-1

FS
type: SiteQuality
SIO_000300: 1.107e0

QD
type: SiteQuality
SIO_000300: 1.296e1

VQSLOD
type: SiteQuality
SIO_000300: 8.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.703e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 14

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

GenotypeQuality
all individuals: 2922
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.803426510369702e-4
allele num: 66540
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.102770657878677e-5
allele num: 16386
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.656814e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 1.589e1

FS
type: SiteQuality
SIO_000300: 3.322e0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
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: 8642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.107243190423842e-5
allele num: 16374
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.656078e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.18e0

MQ
type: SiteQuality
SIO_000300: 5.792e1

QD
type: SiteQuality
SIO_000300: 1.214e1

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

FS
type: SiteQuality
SIO_000300: 4.498e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.649e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16366
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.733402669440111e-4
allele num: 11538
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: 10352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

MQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

DP
type: SiteQuality
SIO_000300: 1.65565e6

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.47e-1

FS
type: SiteQuality
SIO_000300: 1.123e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
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: 1
allele frequency: 6.112469437652811e-5
allele num: 16360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 5.78e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.655871e6

QD
type: SiteQuality
SIO_000300: 1.116e1

FS
type: SiteQuality
SIO_000300: 3.151e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.265e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.678e0

GenotypeQuality
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bin: 5.75e1
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: 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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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009238361770636e-5
allele num: 66462
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

FS
type: SiteQuality
SIO_000300: 1.98e0

MQRankSum
type: SiteQuality
SIO_000300: 5.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 1.65434e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

QD
type: SiteQuality
SIO_000300: 1.163e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15910
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.3e-1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.641896e6

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-2

FS
type: SiteQuality
SIO_000300: 1.913e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.963e1

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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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15870
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.151999999999999e0

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

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

QD
type: SiteQuality
SIO_000300: 1.098e1

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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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15426
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.517727051966974e-5
allele num: 65888
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
allele count: 0
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.837e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1881
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.335113484646195e-4
allele num: 14980
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.046736944732192e-5
allele num: 65644
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.917e1

DP
type: SiteQuality
SIO_000300: 1.605404e6

VQSLOD
type: SiteQuality
SIO_000300: -1.408e0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

FS
type: SiteQuality
SIO_000300: 1.5781e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 8.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14700
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526065193505067e-5
allele num: 65528
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: 9.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

MQ
type: SiteQuality
SIO_000300: 5.929e1

VQSLOD
type: SiteQuality
SIO_000300: -1.78e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.595729e6

QD
type: SiteQuality
SIO_000300: 5.74e0

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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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527977263698316e-5
allele num: 65446
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.67e-1

FS
type: SiteQuality
SIO_000300: 3.045e0

QD
type: SiteQuality
SIO_000300: 1.438e1

MQ
type: SiteQuality
SIO_000300: 5.817e1

DP
type: SiteQuality
SIO_000300: 1.587365e6

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65394
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.663e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.312e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

DP
type: SiteQuality
SIO_000300: 1.582556e6

QD
type: SiteQuality
SIO_000300: 4.74e0

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
all individuals: 7473
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GenotypeQuality
all individuals: 727
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65314
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.985191394244202e-5
allele num: 14316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.284e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.75e-1

FS
type: SiteQuality
SIO_000300: 3.079e0

DP
type: SiteQuality
SIO_000300: 1.575482e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 3.323e1

MQRankSum
type: SiteQuality
SIO_000300: -1.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.78e-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
all individuals: 723
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13966
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.536051119781266e-5
allele num: 65102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.557372e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.29e-1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.914e1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 7.11e-1

BaseQRankSum
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SIO_000300: -6.77e-1

QD
type: SiteQuality
SIO_000300: 1.375e1

MQRankSum
type: SiteQuality
SIO_000300: -1.04e-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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bin: 1.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13254
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10066
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544401544401544e-5
allele num: 64750
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.203e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.15e-1

DP
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.59e0

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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bin: 9.25e1
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
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African
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allele frequency: 9.942334460131238e-5
allele num: 10058
num of homozygotes: 0

South Asian
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European (Finnish)
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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
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.089852923000865e-5
allele num: 64728
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 7.535795026375282e-5
allele num: 13270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.179705846001731e-5
allele num: 64728
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6270
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Latino
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allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10058
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East Asian
type: Population
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allele frequency: 1.171234481143125e-4
allele num: 8538
num of homozygotes: 0

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

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

GenotypeQuality
all individuals: 1822
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2364
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1352
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31005
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13270
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.733624454148471e-5
allele num: 11450
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

FS
type: SiteQuality
SIO_000300: 1.389e0

QD
type: SiteQuality
SIO_000300: 9.94e0

DP
type: SiteQuality
SIO_000300: 1.521699e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

GenotypeQuality
all individuals: 379
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27017
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2668
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2830
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2063
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 7.5e0
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64448
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.90263948158685e-5
allele num: 12654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.15e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.179999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.22e-1

DP
type: SiteQuality
SIO_000300: 1.479878e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.973e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5456
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2624
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1787
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2352
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 494
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3110
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2050
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12348
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.349072116513977e-4
allele num: 8514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64210
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.257e0

QD
type: SiteQuality
SIO_000300: 1.127e1

VQSLOD
type: SiteQuality
SIO_000300: 2.23e0

DP
type: SiteQuality
SIO_000300: 1.448769e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.2e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

GenotypeQuality
all individuals: 1004
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3801
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2227
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1776
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20638
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2285
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2596
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9914
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.35282325425994e-5
allele num: 11972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64016
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.628e0

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-1

DP
type: SiteQuality
SIO_000300: 1.427404e6

QD
type: SiteQuality
SIO_000300: 1.224e1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1