10-49609661-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609661
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609661
    reference: chr 10
allele count: 1
allele frequency: 8.272393368849475e-6
allele num: 120884
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.-43G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.80G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-162G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.-43G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.-43G>T
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11934
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3712
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11903
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5055
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3988
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2780
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

10-49609661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609661
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609661
    reference: chr 10
allele count: 1
allele frequency: 8.272393368849475e-6
allele num: 120884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.-43G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.80G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.-43G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-162G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.-43G>A
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8025
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19978
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3988
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2780
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11903
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

10-49609662-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609662
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609662
    reference: chr 10
allele count: 2
allele frequency: 1.654533421575116e-5
allele num: 120880
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-161G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.81G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.-42G>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11935
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3971
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 713
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11902
  bin: 9.75e1
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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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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 299
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

10-49609662-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609662
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609662
    reference: chr 10
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.-42G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-161G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.-42G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.81G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.-42G>T
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17428
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3971
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5047
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8047
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

10-49609682-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609682
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609682
    reference: chr 10
allele count: 13
allele frequency: 1.074522250876149e-4
allele num: 120984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.-22A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.-22A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.-22A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-141A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.101A>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11989
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8114
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21810
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11899
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3646
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

10-49609694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609694
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609694
    reference: chr 10
allele count: 3
allele frequency: 2.478724283235561e-5
allele num: 121030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.-10G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.-10G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.-10G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.113G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.-10G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-129G>A
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10338
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3896
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22233
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

10-49609697-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609697
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609697
    reference: chr 10
allele count: 3
allele frequency: 2.478314745972738e-5
allele num: 121050
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.-7T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.116T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.-7T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.-7T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.-7T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.-7T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.-7T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.-7T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-126T>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12002
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7082
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22383
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2042
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

10-49609698-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609698
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609698
    reference: chr 10
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.-6G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.-6G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-125G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.-6G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.117G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.-6G>A
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8111
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3631
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-49609699-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609699
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609699
    reference: chr 10
allele count: 2
allele frequency: 1.652127940787734e-5
allele num: 121056
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.-5C>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.-5C>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.-5C>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.-5C>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.-5C>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.-5C>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-124C>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.-5C>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.118C>A
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3635
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3887
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

10-49609703-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609703
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609703
    reference: chr 10
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-120C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.-1C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.-1C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.-1C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.122C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.-1C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.-1C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.-1C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.-1C>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12051
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22618
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3889
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

10-49609708-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609708
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609708
    reference: chr 10
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.127G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.5G>A
  hgvsp: ENSP00000363291.4:p.Ser2Asn
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.5G>A
  hgvsp: ENSP00000363297.3:p.Ser2Asn
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.5G>A
  hgvsp: ENSP00000363289.1:p.Ser2Asn
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.5G>A
  hgvsp: ENSP00000378974.3:p.Ser2Asn
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.5G>A
  hgvsp: ENSP00000387936.1:p.Ser2Asn
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.5G>A
  hgvsp: ENSP00000397729.1:p.Ser2Asn
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.5G>A
  hgvsp: ENSP00000353483.3:p.Ser2Asn
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.5G>A
  hgvsp: ENSP00000363294.3:p.Ser2Asn
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.5G>A
  hgvsp: ENSP00000363304.1:p.Ser2Asn
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-115G>A
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10332
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser2Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

10-49609719-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609719
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609719
    reference: chr 10
allele count: 2
allele frequency: 1.65196418541646e-5
allele num: 121068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.16C>T
  hgvsp: ENSP00000397729.1:p.Arg6Cys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.16C>T
  hgvsp: ENSP00000387936.1:p.Arg6Cys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.16C>T
  hgvsp: ENSP00000353483.3:p.Arg6Cys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.16C>T
  hgvsp: ENSP00000363294.3:p.Arg6Cys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.16C>T
  hgvsp: ENSP00000363297.3:p.Arg6Cys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.16C>T
  hgvsp: ENSP00000363304.1:p.Arg6Cys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.16C>T
  hgvsp: ENSP00000363291.4:p.Arg6Cys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-104C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.16C>T
  hgvsp: ENSP00000378974.3:p.Arg6Cys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.16C>T
  hgvsp: ENSP00000363289.1:p.Arg6Cys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.138C>T
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18358
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg6Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum

10-49609720-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609720
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609720
    reference: chr 10
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.139G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.17G>A
  hgvsp: ENSP00000363294.3:p.Arg6His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-103G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.17G>A
  hgvsp: ENSP00000397729.1:p.Arg6His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.17G>A
  hgvsp: ENSP00000363291.4:p.Arg6His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.17G>A
  hgvsp: ENSP00000378974.3:p.Arg6His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.17G>A
  hgvsp: ENSP00000353483.3:p.Arg6His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.17G>A
  hgvsp: ENSP00000363304.1:p.Arg6His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.17G>A
  hgvsp: ENSP00000363297.3:p.Arg6His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.17G>A
  hgvsp: ENSP00000387936.1:p.Arg6His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.17G>A
  hgvsp: ENSP00000363289.1:p.Arg6His
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg6His
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

10-49609726-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609726
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609726
    reference: chr 10
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.23A>G
  hgvsp: ENSP00000363304.1:p.Asn8Ser
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.23A>G
  hgvsp: ENSP00000363289.1:p.Asn8Ser
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.23A>G
  hgvsp: ENSP00000378974.3:p.Asn8Ser
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.23A>G
  hgvsp: ENSP00000363291.4:p.Asn8Ser
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.145A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.23A>G
  hgvsp: ENSP00000363297.3:p.Asn8Ser
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-97A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.23A>G
  hgvsp: ENSP00000353483.3:p.Asn8Ser
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.23A>G
  hgvsp: ENSP00000363294.3:p.Asn8Ser
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.23A>G
  hgvsp: ENSP00000387936.1:p.Asn8Ser
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.23A>G
  hgvsp: ENSP00000397729.1:p.Asn8Ser
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn8Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

10-49609730-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609730
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609730
    reference: chr 10
allele count: 1
allele frequency: 8.262687356435807e-6
allele num: 121026
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.27T>G
  hgvsp: ENSP00000363289.1:p.Asn9Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.27T>G
  hgvsp: ENSP00000397729.1:p.Asn9Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.27T>G
  hgvsp: ENSP00000378974.3:p.Asn9Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.27T>G
  hgvsp: ENSP00000363297.3:p.Asn9Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.149T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.27T>G
  hgvsp: ENSP00000363291.4:p.Asn9Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.27T>G
  hgvsp: ENSP00000353483.3:p.Asn9Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-93T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.27T>G
  hgvsp: ENSP00000387936.1:p.Asn9Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.27T>G
  hgvsp: ENSP00000363304.1:p.Asn9Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.27T>G
  hgvsp: ENSP00000363294.3:p.Asn9Lys
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18380
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn9Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

10-49609734-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609734
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609734
    reference: chr 10
allele count: 1
allele frequency: 8.263779852904718e-6
allele num: 121010
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.31T>C
  hgvsp: ENSP00000397729.1:p.Tyr11His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.31T>C
  hgvsp: ENSP00000363304.1:p.Tyr11His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-89T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.31T>C
  hgvsp: ENSP00000363291.4:p.Tyr11His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.31T>C
  hgvsp: ENSP00000363297.3:p.Tyr11His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.31T>C
  hgvsp: ENSP00000378974.3:p.Tyr11His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.31T>C
  hgvsp: ENSP00000363289.1:p.Tyr11His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.31T>C
  hgvsp: ENSP00000353483.3:p.Tyr11His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.153T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.31T>C
  hgvsp: ENSP00000363294.3:p.Tyr11His
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.31T>C
  hgvsp: ENSP00000387936.1:p.Tyr11His
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr11His
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

10-49609743-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609743
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609743
    reference: chr 10
allele count: 1
allele frequency: 8.277734549608463e-6
allele num: 120806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.40G>A
  hgvsp: ENSP00000397729.1:p.Glu14Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.40G>A
  hgvsp: ENSP00000363291.4:p.Glu14Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.40G>A
  hgvsp: ENSP00000363289.1:p.Glu14Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.40G>A
  hgvsp: ENSP00000363294.3:p.Glu14Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-80G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.40G>A
  hgvsp: ENSP00000363297.3:p.Glu14Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.40G>A
  hgvsp: ENSP00000353483.3:p.Glu14Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.40G>A
  hgvsp: ENSP00000378974.3:p.Glu14Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.40G>A
  hgvsp: ENSP00000387936.1:p.Glu14Lys
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.162G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.40G>A
  hgvsp: ENSP00000363304.1:p.Glu14Lys
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu14Lys
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

10-49609744-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609744
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609744
    reference: chr 10
allele count: 1
allele frequency: 8.276912380605539e-6
allele num: 120818
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.41A>G
  hgvsp: ENSP00000363291.4:p.Glu14Gly
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.41A>G
  hgvsp: ENSP00000353483.3:p.Glu14Gly
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-79A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.41A>G
  hgvsp: ENSP00000363297.3:p.Glu14Gly
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.41A>G
  hgvsp: ENSP00000397729.1:p.Glu14Gly
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.41A>G
  hgvsp: ENSP00000378974.3:p.Glu14Gly
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.41A>G
  hgvsp: ENSP00000363289.1:p.Glu14Gly
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.163A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.41A>G
  hgvsp: ENSP00000363294.3:p.Glu14Gly
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.41A>G
  hgvsp: ENSP00000363304.1:p.Glu14Gly
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.41A>G
  hgvsp: ENSP00000387936.1:p.Glu14Gly
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu14Gly
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

10-49609751-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609751
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609751
    reference: chr 10
allele count: 26
allele frequency: 2.154493776827591e-4
allele num: 120678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.48A>G
  hgvsp: ENST00000374176.4:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.48A>G
  hgvsp: ENST00000374174.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-72A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.170A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.48A>G
  hgvsp: ENST00000426557.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.48A>G
  hgvsp: ENST00000374179.3:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.48A>G
  hgvsp: ENST00000360332.3:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.48A>G
  hgvsp: ENST00000432379.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.48A>G
  hgvsp: ENST00000374182.3:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.48A>G
  hgvsp: ENST00000374189.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.48A>G
  hgvsp: ENST00000395611.3:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9924
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11980
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7067
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18302
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Gly16Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

10-49609758-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609758
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609758
    reference: chr 10
allele count: 1
allele frequency: 8.301510874979247e-6
allele num: 120460
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.55A>G
  hgvsp: ENSP00000363297.3:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-65A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.55A>G
  hgvsp: ENSP00000397729.1:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.55A>G
  hgvsp: ENSP00000387936.1:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.55A>G
  hgvsp: ENSP00000363304.1:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.55A>G
  hgvsp: ENSP00000378974.3:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.55A>G
  hgvsp: ENSP00000363291.4:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.55A>G
  hgvsp: ENSP00000363289.1:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.177A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.55A>G
  hgvsp: ENSP00000363294.3:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.55A>G
  hgvsp: ENSP00000353483.3:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7061
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr19Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

10-49609766-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609766
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609766
    reference: chr 10
allele count: 1
allele frequency: 8.354498061756449e-6
allele num: 119696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.185A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.63A>G
  hgvsp: ENST00000374176.4:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.63A>G
  hgvsp: ENST00000360332.3:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-57A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.63A>G
  hgvsp: ENST00000374182.3:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.63A>G
  hgvsp: ENST00000432379.1:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.63A>G
  hgvsp: ENST00000395611.3:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.63A>G
  hgvsp: ENST00000374174.1:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.63A>G
  hgvsp: ENST00000374189.1:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.63A>G
  hgvsp: ENST00000374179.3:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.63A>G
  hgvsp: ENST00000426557.1:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr21Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ

10-49609767-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609767
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609767
    reference: chr 10
allele count: 1
allele frequency: 8.380684199058012e-6
allele num: 119322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.64G>A
  hgvsp: ENSP00000363294.3:p.Val22Ile
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.64G>A
  hgvsp: ENSP00000363297.3:p.Val22Ile
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.64G>A
  hgvsp: ENSP00000397729.1:p.Val22Ile
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.64G>A
  hgvsp: ENSP00000363304.1:p.Val22Ile
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.64G>A
  hgvsp: ENSP00000363289.1:p.Val22Ile
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.64G>A
  hgvsp: ENSP00000387936.1:p.Val22Ile
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.64G>A
  hgvsp: ENSP00000363291.4:p.Val22Ile
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.64G>A
  hgvsp: ENSP00000353483.3:p.Val22Ile
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-56G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.186G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.64G>A
  hgvsp: ENSP00000378974.3:p.Val22Ile
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9156
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val22Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-49609774-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609774
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609774
    reference: chr 10
allele count: 1
allele frequency: 8.428150021070375e-6
allele num: 118650
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.71A>C
  hgvsp: ENSP00000363297.3:p.Lys24Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.71A>C
  hgvsp: ENSP00000363289.1:p.Lys24Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.193A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.71A>C
  hgvsp: ENSP00000378974.3:p.Lys24Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.71A>C
  hgvsp: ENSP00000353483.3:p.Lys24Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.71A>C
  hgvsp: ENSP00000397729.1:p.Lys24Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.71A>C
  hgvsp: ENSP00000363291.4:p.Lys24Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.71A>C
  hgvsp: ENSP00000363294.3:p.Lys24Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-49A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.71A>C
  hgvsp: ENSP00000363304.1:p.Lys24Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.71A>C
  hgvsp: ENSP00000387936.1:p.Lys24Thr
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11585
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys24Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-49609775-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609775
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609775
    reference: chr 10
allele count: 1
allele frequency: 8.439530762089629e-6
allele num: 118490
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.72A>G
  hgvsp: ENST00000374179.3:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.72A>G
  hgvsp: ENST00000374176.4:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.72A>G
  hgvsp: ENST00000426557.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.72A>G
  hgvsp: ENST00000360332.3:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.72A>G
  hgvsp: ENST00000432379.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.194A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.72A>G
  hgvsp: ENST00000374174.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.72A>G
  hgvsp: ENST00000395611.3:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.72A>G
  hgvsp: ENST00000374189.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.72A>G
  hgvsp: ENST00000374182.3:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-48A>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys24Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

10-49609777-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609777
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609777
    reference: chr 10
allele count: 1
allele frequency: 8.452228007302725e-6
allele num: 118312
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.74G>A
  hgvsp: ENSP00000363304.1:p.Arg25Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.74G>A
  hgvsp: ENSP00000397729.1:p.Arg25Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.74G>A
  hgvsp: ENSP00000363291.4:p.Arg25Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.74G>A
  hgvsp: ENSP00000363289.1:p.Arg25Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.196G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.74G>A
  hgvsp: ENSP00000363297.3:p.Arg25Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.74G>A
  hgvsp: ENSP00000378974.3:p.Arg25Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.74G>A
  hgvsp: ENSP00000353483.3:p.Arg25Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.74G>A
  hgvsp: ENSP00000387936.1:p.Arg25Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.74G>A
  hgvsp: ENSP00000363294.3:p.Arg25Gln
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg25Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

10-49609808-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609808
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609808
    reference: chr 10
allele count: 1
allele frequency: 8.708373972411871e-6
allele num: 114832
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.105A>G
  hgvsp: ENST00000374176.4:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.105A>G
  hgvsp: ENST00000374189.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.105A>G
  hgvsp: ENST00000374174.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.105A>G
  hgvsp: ENST00000360332.3:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.105A>G
  hgvsp: ENST00000426557.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.105A>G
  hgvsp: ENST00000395611.3:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.105A>G
  hgvsp: ENST00000432379.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.105A>G
  hgvsp: ENST00000374179.3:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.105A>G
  hgvsp: ENST00000374182.3:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-15A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.227A>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly35Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

10-49609811-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609811
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609811
    reference: chr 10
allele count: 10
allele frequency: 8.73179420907408e-5
allele num: 114524
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.108T>C
  hgvsp: ENST00000432379.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.108T>C
  hgvsp: ENST00000374174.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.108T>C
  hgvsp: ENST00000360332.3:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.-12T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.108T>C
  hgvsp: ENST00000374176.4:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.108T>C
  hgvsp: ENST00000395611.3:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.108T>C
  hgvsp: ENST00000426557.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.108T>C
  hgvsp: ENST00000374179.3:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.108T>C
  hgvsp: ENST00000374182.3:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.108T>C
  hgvsp: ENST00000374189.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.230T>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11260
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15761
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala36Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

10-49609825-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609825
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609825
    reference: chr 10
allele count: 1
allele frequency: 8.850810734263259e-6
allele num: 112984
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.244G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.122G>A
  hgvsp: ENSP00000363297.3:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.122G>A
  hgvsp: ENSP00000387936.1:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3G>A
  hgvsp: ENSP00000393223.1:p.Met1?
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.122G>A
  hgvsp: ENSP00000363294.3:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.122G>A
  hgvsp: ENSP00000353483.3:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.122G>A
  hgvsp: ENSP00000363304.1:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.122G>A
  hgvsp: ENSP00000378974.3:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.122G>A
  hgvsp: ENSP00000363291.4:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.122G>A
  hgvsp: ENSP00000397729.1:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.122G>A
  hgvsp: ENSP00000363289.1:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/6881
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

10-49609834-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609834
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609834
    reference: chr 10
allele count: 1
allele frequency: 8.90805109658109e-6
allele num: 112258
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.122+9T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.244+9T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.122+9T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.122+9T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+9T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.122+9T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.122+9T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.122+9T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.122+9T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.122+9T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.122+9T>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

10-49609836-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609836
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609836
    reference: chr 10
allele count: 1
allele frequency: 8.922835320151331e-6
allele num: 112072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.122+11A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.244+11A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.122+11A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.122+11A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.122+11A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.122+11A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.122+11A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+11A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.122+11A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.122+11A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.122+11A>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3792
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

10-49609840-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609840
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609840
    reference: chr 10
allele count: 1
allele frequency: 8.94566403664144e-6
allele num: 111786
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.122+15C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.122+15C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+15C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.122+15C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.122+15C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.122+15C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.122+15C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.122+15C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.244+15C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.122+15C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.122+15C>T
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11122
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

10-49609853-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609853
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609853
    reference: chr 10
allele count: 1
allele frequency: 9.013881377321074e-6
allele num: 110940
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.122+28A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+28A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.122+28A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.122+28A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.122+28A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.122+28A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.122+28A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.122+28A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.122+28A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.122+28A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.244+28A>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2721
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

10-49609854-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609854
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609854
    reference: chr 10
allele count: 1
allele frequency: 9.02429339782695e-6
allele num: 110812
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.122+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.122+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.122+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.122+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.122+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.122+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.122+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.244+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.122+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.122+29A>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD

10-49609869-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49609869
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49609869
    reference: chr 10
allele count: 1
allele frequency: 9.071940488070398e-6
allele num: 110230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.122+44C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.122+44C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+44C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.122+44C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.244+44C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.122+44C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.122+44C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.122+44C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.122+44C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.122+44C>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.122+44C>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/10-49612844-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612844
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612844
    reference: chr 10
allele count: 9495
allele frequency: 8.144062853809998e-2
allele num: 116588
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123-51A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123-51A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3019A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123-51A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123-51A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123-51A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123-51A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123-51A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123-51A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123-51A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245-51A>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 7.5e0
  variant carriers: 266
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 3.25e1
  variant carriers: 1350
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 1.75e1
  variant carriers: 1028
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 12996
  bin: 2.25e1
  variant carriers: 1249
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 224
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 3.75e1
  variant carriers: 970
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 1.25e1
  variant carriers: 754
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.75e1
  variant carriers: 429
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 151
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 19506
  bin: 2.75e1
  variant carriers: 1401
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 4.25e1
  variant carriers: 653
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 2.75e1
  variant carriers: 15
num of homozygotes: 869
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-49612847-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612847
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612847
    reference: chr 10
allele count: 3
allele frequency: 2.565593678377176e-5
allele num: 116932
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245-48G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123-48G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3022G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123-48G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123-48G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123-48G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123-48G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123-48G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123-48G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123-48G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123-48G>A
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14787
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21593
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

10-49612850-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612850
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612850
    reference: chr 10
allele count: 1
allele frequency: 8.539126276599378e-6
allele num: 117108
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123-45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123-45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123-45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123-45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123-45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123-45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123-45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123-45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123-45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245-45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3025T>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

10-49612857-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612857
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612857
    reference: chr 10
allele count: 1
allele frequency: 8.527184664711099e-6
allele num: 117272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245-38T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3032T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123-38T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123-38T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123-38T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123-38T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123-38T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123-38T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123-38T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123-38T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123-38T>A
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

10-49612863-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612863
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612863
    reference: chr 10
allele count: 4
allele frequency: 3.402517863218782e-5
allele num: 117560
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3038T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123-32T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123-32T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123-32T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123-32T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123-32T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123-32T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245-32T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123-32T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123-32T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123-32T>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

10-49612869-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612869
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612869
    reference: chr 10
allele count: 2
allele frequency: 1.695231314312838e-5
allele num: 117978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123-26G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245-26G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123-26G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123-26G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123-26G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123-26G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123-26G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123-26G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123-26G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3044G>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123-26G>T
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20310
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

10-49612879-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612879
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612879
    reference: chr 10
allele count: 1
allele frequency: 8.417083312290625e-6
allele num: 118806
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123-16G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3054G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123-16G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123-16G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123-16G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123-16G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123-16G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123-16G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123-16G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123-16G>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245-16G>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-49612880-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612880
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612880
    reference: chr 10
allele count: 1
allele frequency: 8.410853365182432e-6
allele num: 118894
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123-15A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123-15A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123-15A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123-15A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123-15A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3055A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123-15A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123-15A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245-15A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123-15A>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123-15A>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

10-49612880-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612880
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612880
    reference: chr 10
allele count: 1
allele frequency: 8.410853365182432e-6
allele num: 118894
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123-15A>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123-15A>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123-15A>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123-15A>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123-15A>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3055A>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123-15A>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123-15A>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123-15A>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245-15A>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123-15A>T
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

10-49612883-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612883
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612883
    reference: chr 10
allele count: 1
allele frequency: 8.391937026904549e-6
allele num: 119162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123-12T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123-12T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3058T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123-12T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123-12T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245-12T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123-12T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123-12T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123-12T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123-12T>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123-12T>A
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

10-49612889-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612889
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612889
    reference: chr 10
allele count: 2
allele frequency: 1.670257720766314e-5
allele num: 119742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123-6T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123-6T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123-6T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123-6T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3064T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123-6T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123-6T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123-6T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245-6T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123-6T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123-6T>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23668
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22657
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.123-6T>C
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-49612895-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612895
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612895
    reference: chr 10
allele count: 1
allele frequency: 8.317253310266817e-6
allele num: 120232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.123C>T
  hgvsp: ENST00000426557.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.123C>T
  hgvsp: ENST00000360332.3:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.123C>T
  hgvsp: ENST00000374174.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.123C>T
  hgvsp: ENST00000374189.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.123C>T
  hgvsp: ENST00000432379.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.123C>T
  hgvsp: ENST00000374179.3:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.123C>T
  hgvsp: ENST00000374176.4:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3070C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.123C>T
  hgvsp: ENST00000374182.3:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.245C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.123C>T
  hgvsp: ENST00000395611.3:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.123C>T
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

10-49612896-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612896
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612896
    reference: chr 10
allele count: 1
allele frequency: 8.304958059961797e-6
allele num: 120410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.124G>A
  hgvsp: ENSP00000363297.3:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.124G>A
  hgvsp: ENSP00000363289.1:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.124G>A
  hgvsp: ENSP00000353483.3:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.124G>A
  hgvsp: ENSP00000363294.3:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.124G>A
  hgvsp: ENSP00000363304.1:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.124G>A
  hgvsp: ENSP00000397729.1:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.246G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.124G>A
  hgvsp: ENSP00000387936.1:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.124G>A
  hgvsp: ENSP00000378974.3:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3071G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.124G>A
  hgvsp: ENSP00000363291.4:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala42Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

10-49612908-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612908
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612908
    reference: chr 10
allele count: 2
allele frequency: 1.653411815280832e-5
allele num: 120962
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.136G>A
  hgvsp: ENSP00000378974.3:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.136G>A
  hgvsp: ENSP00000363297.3:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.136G>A
  hgvsp: ENSP00000363294.3:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.136G>A
  hgvsp: ENSP00000363291.4:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.136G>A
  hgvsp: ENSP00000397729.1:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.136G>A
  hgvsp: ENSP00000363289.1:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.136G>A
  hgvsp: ENSP00000353483.3:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.136G>A
  hgvsp: ENSP00000363304.1:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.136G>A
  hgvsp: ENSP00000387936.1:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3083G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.258G>A
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala46Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

10-49612909-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612909
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612909
    reference: chr 10
allele count: 1
allele frequency: 8.265145879824779e-6
allele num: 120990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.137C>T
  hgvsp: ENSP00000378974.3:p.Ala46Val
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.137C>T
  hgvsp: ENSP00000363297.3:p.Ala46Val
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.137C>T
  hgvsp: ENSP00000353483.3:p.Ala46Val
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.137C>T
  hgvsp: ENSP00000363304.1:p.Ala46Val
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.137C>T
  hgvsp: ENSP00000363289.1:p.Ala46Val
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.137C>T
  hgvsp: ENSP00000363291.4:p.Ala46Val
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.137C>T
  hgvsp: ENSP00000397729.1:p.Ala46Val
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3084C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.259C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.137C>T
  hgvsp: ENSP00000387936.1:p.Ala46Val
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.137C>T
  hgvsp: ENSP00000363294.3:p.Ala46Val
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala46Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

10-49612915-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612915
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612915
    reference: chr 10
allele count: 5
allele frequency: 4.12779658218443e-5
allele num: 121130
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.143T>C
  hgvsp: ENSP00000363291.4:p.Leu48Pro
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.143T>C
  hgvsp: ENSP00000363294.3:p.Leu48Pro
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.143T>C
  hgvsp: ENSP00000378974.3:p.Leu48Pro
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.265T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.143T>C
  hgvsp: ENSP00000363297.3:p.Leu48Pro
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.143T>C
  hgvsp: ENSP00000387936.1:p.Leu48Pro
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.143T>C
  hgvsp: ENSP00000353483.3:p.Leu48Pro
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.143T>C
  hgvsp: ENSP00000363289.1:p.Leu48Pro
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.143T>C
  hgvsp: ENSP00000363304.1:p.Leu48Pro
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3090T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.143T>C
  hgvsp: ENSP00000397729.1:p.Leu48Pro
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu48Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

10-49612916-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612916
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612916
    reference: chr 10
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.144T>C
  hgvsp: ENST00000374176.4:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.266T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.144T>C
  hgvsp: ENST00000360332.3:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.144T>C
  hgvsp: ENST00000374182.3:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.144T>C
  hgvsp: ENST00000395611.3:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.144T>C
  hgvsp: ENST00000426557.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.144T>C
  hgvsp: ENST00000374179.3:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.144T>C
  hgvsp: ENST00000374189.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.144T>C
  hgvsp: ENST00000374174.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.144T>C
  hgvsp: ENST00000432379.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3091T>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu48Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

10-49612947-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612947
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612947
    reference: chr 10
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.297C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.175C>T
  hgvsp: ENSP00000387936.1:p.Arg59Ter
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.175C>T
  hgvsp: ENSP00000363304.1:p.Arg59Ter
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.175C>T
  hgvsp: ENSP00000363294.3:p.Arg59Ter
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.175C>T
  hgvsp: ENSP00000363291.4:p.Arg59Ter
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.175C>T
  hgvsp: ENSP00000363289.1:p.Arg59Ter
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.175C>T
  hgvsp: ENSP00000363297.3:p.Arg59Ter
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.175C>T
  hgvsp: ENSP00000397729.1:p.Arg59Ter
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.175C>T
  hgvsp: ENSP00000378974.3:p.Arg59Ter
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3122C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.175C>T
  hgvsp: ENSP00000353483.3:p.Arg59Ter
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg59Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

10-49612948-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612948
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612948
    reference: chr 10
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.176G>A
  hgvsp: ENSP00000378974.3:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.176G>A
  hgvsp: ENSP00000363297.3:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.176G>A
  hgvsp: ENSP00000387936.1:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.176G>A
  hgvsp: ENSP00000363289.1:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.298G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.176G>A
  hgvsp: ENSP00000397729.1:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3123G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.176G>A
  hgvsp: ENSP00000353483.3:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.176G>A
  hgvsp: ENSP00000363291.4:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.176G>A
  hgvsp: ENSP00000363294.3:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.176G>A
  hgvsp: ENSP00000363304.1:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg59Gln
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

10-49612952-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49612952
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49612952
    reference: chr 10
allele count: 6
allele frequency: 4.945435363159804e-5
allele num: 121324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.180A>G
  hgvsp: ENST00000395611.3:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.180A>G
  hgvsp: ENST00000374174.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.180A>G
  hgvsp: ENST00000360332.3:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.180A>G
  hgvsp: ENST00000374182.3:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.302A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3127A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.180A>G
  hgvsp: ENST00000374176.4:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.180A>G
  hgvsp: ENST00000426557.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.180A>G
  hgvsp: ENST00000374179.3:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.180A>G
  hgvsp: ENST00000432379.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.180A>G
  hgvsp: ENST00000374189.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7087
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro60Pro
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

10-49613033-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49613033
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49613033
    reference: chr 10
allele count: 3
allele frequency: 2.533056385835149e-5
allele num: 118434
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.252+9A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.252+9A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.252+9A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.252+9A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.374+9A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.252+9A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.252+9A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.252+9A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.252+9A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3208A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.252+9A>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22398
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19005
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3563
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

10-49613034-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49613034
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49613034
    reference: chr 10
allele count: 1
allele frequency: 8.455372543714276e-6
allele num: 118268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.252+10C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.252+10C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.252+10C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.252+10C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.252+10C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.252+10C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3209C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.252+10C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.374+10C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.252+10C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.252+10C>T
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/10-49613034-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49613034
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49613033
    reference: chr 10
allele count: 1
allele frequency: 8.455372543714276e-6
allele num: 118268
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.252+11delA
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.252+11delA
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.252+11delA
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.252+11delA
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.252+11delA
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.252+11delA
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.252+11delA
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.252+11delA
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.252+11delA
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.374+11delA
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3210delA
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: CA
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

10-49613043-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49613043
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49613043
    reference: chr 10
allele count: 13
allele frequency: 1.110067457945521e-4
allele num: 117110
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.252+19T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.252+19T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.252+19T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.252+19T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.252+19T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.374+19T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.252+19T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.252+19T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.252+19T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.252+19T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3218T>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19620
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15904
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

10-49613053-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49613053
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49613053
    reference: chr 10
allele count: 1
allele frequency: 8.605111436193099e-6
allele num: 116210
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.252+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.252+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.252+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.252+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.252+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.252+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3228A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.374+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.252+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.252+29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.252+29A>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12395
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

10-49613058-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49613058
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49613059
    reference: chr 10
allele count: 11
allele frequency: 9.493725510503512e-5
allele num: 115866
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.252+35dupG
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.374+35dupG
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.252+35dupG
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.252+35dupG
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.252+35dupG
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3234dupG
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.252+35dupG
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.252+35dupG
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.252+35dupG
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.252+35dupG
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.252+35dupG
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12365
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11463
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13120
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4371
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11174
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6331
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

10-49613069-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49613069
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49613069
    reference: chr 10
allele count: 3
allele frequency: 2.626970227670753e-5
allele num: 114200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.252+45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.252+45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.252+45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.252+45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.252+45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.252+45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.252+45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.252+45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.374+45T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3244T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.252+45T>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15897
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12128
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7197
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

10-49613070-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49613070
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49613070
    reference: chr 10
allele count: 4
allele frequency: 3.50938761186173e-5
allele num: 113980
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.252+46T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.252+46T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.252+46T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.252+46T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.252+46T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.252+46T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.252+46T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.252+46T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.252+46T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3245T>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.374+46T>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8197
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11969
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15879
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

10-49613071-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49613071
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49613071
    reference: chr 10
allele count: 1
allele frequency: 8.869336928371234e-6
allele num: 112748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3246T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.374+47T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.252+47T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.252+47T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.252+47T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.252+47T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.252+47T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.252+47T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.252+47T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.252+47T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.252+47T>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13115
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

10-49613072-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49613072
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49613073
    reference: chr 10
allele count: 14
allele frequency: 1.239464551313832e-4
allele num: 112952
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.252+50dupT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.252+50dupT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.252+50dupT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.252+50dupT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.252+50dupT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.374+50dupT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.252+50dupT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.252+50dupT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.252+50dupT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.252+50dupT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3249dupT
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11893
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13142
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15803
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5996
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum

10-49613075-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49613075
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49613075
    reference: chr 10
allele count: 2
allele frequency: 1.781039058186546e-5
allele num: 112294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.374+51C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.3+3250C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.252+51C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.252+51C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.252+51C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.252+51C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.252+51C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.252+51C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.252+51C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.252+51C>T
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.252+51C>T
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15738
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13241
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4667
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS

10-49617879-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49617879
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49617879
    reference: chr 10
allele count: 1
allele frequency: 1.335969646769625e-5
allele num: 74852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.253-43T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.253-43T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.253-43T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.375-43T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.253-43T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.253-43T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.253-43T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.253-43T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.253-43T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.4-43T>C
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.253-43T>C
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

10-49617893-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49617893
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49617893
    reference: chr 10
allele count: 17
allele frequency: 2.166985340981517e-4
allele num: 78450
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.253-29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.253-29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.253-29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.253-29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.253-29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.253-29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.4-29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.253-29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.253-29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.253-29A>G
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.375-29A>G
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19029
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11013
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16364
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

10-49617899-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49617899
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49617897
    reference: chr 10
allele count: 1
allele frequency: 1.215598560731304e-5
allele num: 82264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.253-21_253-20delGT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl transcript: ENST00000476134
  gene symbol: MAPK8
  hgvsc: ENST00000476134.1:n.375-21_375-20delGT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.253-21_253-20delGT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363304
  ensembl transcript: ENST00000374189
  gene symbol: MAPK8
  hgvsc: ENST00000374189.1:c.253-21_253-20delGT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363291
  ensembl transcript: ENST00000374176
  gene symbol: MAPK8
  hgvsc: ENST00000374176.4:c.253-21_253-20delGT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000387936
  ensembl transcript: ENST00000432379
  gene symbol: MAPK8
  hgvsc: ENST00000432379.1:c.253-21_253-20delGT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363294
  ensembl transcript: ENST00000374179
  gene symbol: MAPK8
  hgvsc: ENST00000374179.3:c.253-21_253-20delGT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000353483
  ensembl transcript: ENST00000360332
  gene symbol: MAPK8
  hgvsc: ENST00000360332.3:c.253-21_253-20delGT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000378974
  ensembl transcript: ENST00000395611
  gene symbol: MAPK8
  hgvsc: ENST00000395611.3:c.253-21_253-20delGT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000393223
  ensembl transcript: ENST00000429041
  gene symbol: MAPK8
  hgvsc: ENST00000429041.1:c.4-21_4-20delGT
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000397729
  ensembl transcript: ENST00000426557
  gene symbol: MAPK8
  hgvsc: ENST00000426557.1:c.253-21_253-20delGT
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17921
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7994
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: CTG
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

10-49617901-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49617901
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 49617901
    reference: chr 10
allele count: 26
allele frequency: 3.090822634331907e-4
allele num: 84120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363289
  ensembl transcript: ENST00000374174
  gene symbol: MAPK8
  hgvsc: ENST00000374174.1:c.253-21G>A
  variant of: http://identifiers.org/hgnc/6881
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000107643
  ensembl protein: ENSP00000363297
  ensembl transcript: ENST00000374182
  gene symbol: MAPK8
  hgvsc: ENST00000374182.3:c.253-21G>A
  variant of: http://identifiers.org/hgnc/6881
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 496
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8025
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19978
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.493e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.351e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.89e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.869e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.069062e6

QD
type: SiteQuality
SIO_000300: 7.73e0

GenotypeQuality
all individuals: 3712
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5055
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2052
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.351e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.069062e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.869e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 2.493e0

MQRankSum
type: SiteQuality
SIO_000300: 1.89e0

QD
type: SiteQuality
SIO_000300: 7.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.54e-1

GenotypeQuality
all individuals: 8047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3717
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007066606525334e-5
allele num: 66510
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.387e1

VQSLOD
type: SiteQuality
SIO_000300: -1.537e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

DP
type: SiteQuality
SIO_000300: 2.069499e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 1.1522e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.55e-1

GenotypeQuality
all individuals: 20026
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11902
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2054
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3717
bin: 7.25e1
variant carriers: 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: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503533303262667e-5
allele num: 66510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.069499e6

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

FS
type: SiteQuality
SIO_000300: 1.1522e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

QD
type: SiteQuality
SIO_000300: 1.387e1

VQSLOD
type: SiteQuality
SIO_000300: -1.537e0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4951
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3905
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 12
allele frequency: 1.165954139137194e-3
allele num: 10292
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502674761074713e-5
allele num: 66548
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 2.694e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

QD
type: SiteQuality
SIO_000300: 1.186e1

DP
type: SiteQuality
SIO_000300: 2.081118e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.713e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-1

GenotypeQuality
all individuals: 8110
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
all individuals: 142
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variant carriers: 0

GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
all individuals: 11893
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variant carriers: 3

GenotypeQuality
all individuals: 181
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variant carriers: 0

GenotypeQuality
all individuals: 2041
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2752
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3637
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.313208420078649e-4
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.082725060827251e-5
allele num: 16440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.084563e6

VQSLOD
type: SiteQuality
SIO_000300: -4.52e-1

QD
type: SiteQuality
SIO_000300: 1.276e1

MQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.04e-1

FS
type: SiteQuality
SIO_000300: 1.0256e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.082e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 8132
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variant carriers: 0

GenotypeQuality
all individuals: 265
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variant carriers: 0

GenotypeQuality
all individuals: 2752
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3895
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variant carriers: 0

GenotypeQuality
all individuals: 3639
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11891
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variant carriers: 3

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4917
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.506399086703119e-5
allele num: 66572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.085279e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

FS
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.3e-2

QD
type: SiteQuality
SIO_000300: 1.21e1

MQ
type: SiteQuality
SIO_000300: 5.923e1

GenotypeQuality
all individuals: 91
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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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
all individuals: 2040
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11888
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.085877e6

FS
type: SiteQuality
SIO_000300: 3.078e0

QD
type: SiteQuality
SIO_000300: 1.882e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.839e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.454e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.748e0

GenotypeQuality
all individuals: 178
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 2041
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004266057802079e-5
allele num: 66572
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

FS
type: SiteQuality
SIO_000300: 5.83e0

VQSLOD
type: SiteQuality
SIO_000300: 8.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.645e0

QD
type: SiteQuality
SIO_000300: 1.207e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-2

DP
type: SiteQuality
SIO_000300: 2.086407e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.75e1
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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variant carriers: 0

GenotypeQuality
all individuals: 4
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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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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 8.779999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.522e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.47e-1

FS
type: SiteQuality
SIO_000300: 1.1021e1

MQRankSum
type: SiteQuality
SIO_000300: -4.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.51e0

DP
type: SiteQuality
SIO_000300: 2.087624e6

GenotypeDepth
all individuals: 800
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4901
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variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.75e1
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GenotypeQuality
all individuals: 8109
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11884
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variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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South Asian
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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African
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South Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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MQ
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FS
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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East Asian
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South Asian
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MQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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DP
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FS
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

Latino
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African
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East Asian
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European (Finnish)
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Other
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South Asian
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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South Asian
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African
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East Asian
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European (Non-Finnish)
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Latino
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Other
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MQRankSum
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ClippingRankSum
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MQ
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QD
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FS
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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MQ
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QD
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FS
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Finnish)
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Latino
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Other
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European (Non-Finnish)
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ReadPosRankSum
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QD
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FS
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VQSLOD
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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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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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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
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
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.45e-1

VQSLOD
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 1.67e-2

BaseQRankSum
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SIO_000300: -1.312e0

QD
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SIO_000300: 8.220000000000001e0

ClippingRankSum
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SIO_000300: -1.49e-1

MQRankSum
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SIO_000300: -6.69e-1

FS
type: SiteQuality
SIO_000300: 4.658e0

DP
type: SiteQuality
SIO_000300: 2.083647e6

GenotypeDepth
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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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variant carriers: 26

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

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

Latino
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allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

European (Non-Finnish)
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allele count: 20
allele frequency: 3.007518796992481e-4
allele num: 66500
num of homozygotes: 0

South Asian
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allele frequency: 3.102121851346321e-4
allele num: 16118
num of homozygotes: 0

Other
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VQSLOD
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SIO_000300: 2.01e0

ClippingRankSum
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DP
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BaseQRankSum
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MQRankSum
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SIO_000300: -8.1e-2

InbreedingCoeff
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SIO_000300: 8.6e-3

ReadPosRankSum
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FS
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SIO_000300: 5.25e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
type: SiteQuality
SIO_000300: 1.257e1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.504800312998465e-5
allele num: 66454
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 15954
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

BaseQRankSum
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SIO_000300: 4.74e0

InbreedingCoeff
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SIO_000300: 1.61e-2

DP
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SIO_000300: 2.077185e6

QD
type: SiteQuality
SIO_000300: 1.279e1

FS
type: SiteQuality
SIO_000300: 1.114e0

VQSLOD
type: SiteQuality
SIO_000300: 2.56e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.467e0

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 15424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66252
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

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

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

African
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: -1.76e-1

VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: -4.85e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.064311e6

QD
type: SiteQuality
SIO_000300: 6.56e0

FS
type: SiteQuality
SIO_000300: 2.933e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4770
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GenotypeQuality
all individuals: 200
bin: 4.75e1
variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.511213201958532e-5
allele num: 66172
num of homozygotes: 0

Latino
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Other
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South Asian
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: -1.208e0

DP
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QD
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 9.370000000000001e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65982
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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ClippingRankSum
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DP
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QD
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 1

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

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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Other
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Latino
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South Asian
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ReadPosRankSum
type: SiteQuality
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QD
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MQ
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10348
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65906
num of homozygotes: 0

European (Finnish)
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allele count: 1
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allele num: 6606
num of homozygotes: 0

Other
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East Asian
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Latino
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South Asian
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

FS
type: SiteQuality
SIO_000300: 1.5724e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

QD
type: SiteQuality
SIO_000300: 1.315e1

DP
type: SiteQuality
SIO_000300: 2.039159e6

VQSLOD
type: SiteQuality
SIO_000300: -2.033e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 2238
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3997
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2734
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3419
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3812
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11850
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7246
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4687
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18656
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.538224888478696e-5
allele num: 65010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12056
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.11e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 1.458e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.069e0

DP
type: SiteQuality
SIO_000300: 1.997289e6

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

FS
type: SiteQuality
SIO_000300: 8.417e0

VQSLOD
type: SiteQuality
SIO_000300: 2.57e-1

GenotypeDepth
all individuals: 6993
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18698
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4063
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2731
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3411
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4672
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3810
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11855
bin: 9.75e1
variant carriers: 10

Latino
type: Population
allele count: 2
allele frequency: 1.742160278745645e-4
allele num: 11480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166316771635176e-4
allele num: 8574
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.814641744548286e-4
allele num: 10272
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.145e1

MQRankSum
type: SiteQuality
SIO_000300: -2.26e-1

FS
type: SiteQuality
SIO_000300: 3.445e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

DP
type: SiteQuality
SIO_000300: 1.995406e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 581
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1372
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 721
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7126
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
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variant carriers: 0

GenotypeQuality
all individuals: 3580
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2732
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18387
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4639
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3378
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3808
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11841
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2000
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.769441187964049e-5
allele num: 10236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64536
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10758
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: 4.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.81e-1

DP
type: SiteQuality
SIO_000300: 1.982898e6

FS
type: SiteQuality
SIO_000300: 8.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.532e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.614e1

GenotypeQuality
all individuals: 3367
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3216
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18090
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3794
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11839
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4622
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7097
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554146462762651e-5
allele num: 64344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.98e0

FS
type: SiteQuality
SIO_000300: 5.673e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.27e-1

DP
type: SiteQuality
SIO_000300: 1.973349e6

MQ
type: SiteQuality
SIO_000300: 5.937e1

GenotypeQuality
all individuals: 304
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7080
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3023
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3358
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17828
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11839
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4617
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555306706482518e-5
allele num: 64296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.206e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-2

MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.67e-1

FS
type: SiteQuality
SIO_000300: 2.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

DP
type: SiteQuality
SIO_000300: 1.970472e6

GenotypeQuality
all individuals: 260
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3786
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3333
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variant carriers: 0

GenotypeQuality
all individuals: 2880
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4593
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variant carriers: 0

GenotypeQuality
all individuals: 2089
bin: 7.5e0
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GenotypeQuality
all individuals: 150
bin: 2.5e0
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GenotypeQuality
all individuals: 17741
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 8.75e1
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GenotypeQuality
all individuals: 11836
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10026
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557875058420315e-5
allele num: 64190
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.302e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: -3.618e-1

FS
type: SiteQuality
SIO_000300: 9.42e0

DP
type: SiteQuality
SIO_000300: 1.96672e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

QD
type: SiteQuality
SIO_000300: 1.424e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 289
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6802
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variant carriers: 0

GenotypeQuality
all individuals: 2754
bin: 7.5e0
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GenotypeQuality
all individuals: 666
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variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 5.25e1
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GenotypeQuality
all individuals: 480
bin: 2.75e1
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GenotypeQuality
all individuals: 486
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 4.25e1
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GenotypeQuality
all individuals: 128
bin: 5.75e1
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GenotypeQuality
all individuals: 139
bin: 2.5e0
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GenotypeQuality
all individuals: 16951
bin: 6.25e1
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GenotypeQuality
all individuals: 3763
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11827
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2276
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4535
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1980
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562841871659425e-5
allele num: 63986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.13e-1

DP
type: SiteQuality
SIO_000300: 1.945747e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.14e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: 5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e-1

GenotypeQuality
all individuals: 520
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 2.5e0
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GenotypeQuality
all individuals: 2801
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4525
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 810
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63964
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.173984503404555e-4
allele num: 8518
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.291e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

FS
type: SiteQuality
SIO_000300: 1.744e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.99e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.940531e6

VQSLOD
type: SiteQuality
SIO_000300: -5.072e-1

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

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

GenotypeQuality
all individuals: 1055
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1889
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 478
bin: 5.75e1
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GenotypeQuality
all individuals: 1963
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.936406995230525e-5
allele num: 10064
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.117e0

QD
type: SiteQuality
SIO_000300: 1.072e1

DP
type: SiteQuality
SIO_000300: 1.908208e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

GenotypeQuality
all individuals: 1610
bin: 7.25e1
variant carriers: 63

GenotypeQuality
all individuals: 2079
bin: 4.75e1
variant carriers: 62

GenotypeQuality
all individuals: 2052
bin: 7.75e1
variant carriers: 105

GenotypeQuality
all individuals: 245
bin: 2.5e0
variant carriers: 7

GenotypeQuality
all individuals: 11324
bin: 9.75e1
variant carriers: 7971

GenotypeQuality
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bin: 1.25e1
variant carriers: 11

GenotypeQuality
all individuals: 5573
bin: 6.75e1
variant carriers: 76

GenotypeQuality
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variant carriers: 57

GenotypeQuality
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bin: 4.25e1
variant carriers: 43

GenotypeQuality
all individuals: 1317
bin: 2.25e1
variant carriers: 38

GenotypeQuality
all individuals: 221
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variant carriers: 9

GenotypeQuality
all individuals: 1271
bin: 8.25e1
variant carriers: 85

GenotypeQuality
all individuals: 1521
bin: 3.25e1
variant carriers: 31

GenotypeQuality
all individuals: 1144
bin: 5.75e1
variant carriers: 42

GenotypeQuality
all individuals: 562
bin: 8.75e1
variant carriers: 84

GenotypeQuality
all individuals: 764
bin: 9.25e1
variant carriers: 95

GenotypeQuality
all individuals: 1842
bin: 3.75e1
variant carriers: 52

GenotypeQuality
all individuals: 2307
bin: 5.25e1
variant carriers: 65

GenotypeQuality
all individuals: 449
bin: 1.75e1
variant carriers: 20

South Asian
type: Population
allele count: 2575
allele frequency: 1.758639530118836e-1
allele num: 14642
num of homozygotes: 271

Latino
type: Population
allele count: 3245
allele frequency: 2.849490691956446e-1
allele num: 11388
num of homozygotes: 509

East Asian
type: Population
allele count: 244
allele frequency: 2.856473893701709e-2
allele num: 8542
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2946
allele frequency: 4.536634944100527e-2
allele num: 64938
num of homozygotes: 74

European (Finnish)
type: Population
allele count: 284
allele frequency: 4.303030303030303e-2
allele num: 6600
num of homozygotes: 9

African
type: Population
allele count: 143
allele frequency: 1.487723678734915e-2
allele num: 9612
num of homozygotes: 2

Other
type: Population
allele count: 58
allele frequency: 6.697459584295612e-2
allele num: 866
num of homozygotes: 3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.796e1

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

DP
type: SiteQuality
SIO_000300: 1.634258e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.760000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

GenotypeQuality
all individuals: 1767
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2282
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
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variant carriers: 0

GenotypeQuality
all individuals: 229
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variant carriers: 0

GenotypeQuality
all individuals: 6491
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variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
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variant carriers: 0

GenotypeQuality
all individuals: 3732
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 30975
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variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1757
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
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variant carriers: 0

GenotypeQuality
all individuals: 974
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.609852792034174e-5
allele num: 65078
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.983e0

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

QD
type: SiteQuality
SIO_000300: 1.634e1

DP
type: SiteQuality
SIO_000300: 1.585131e6

GenotypeQuality
all individuals: 201
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1734
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32680
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variant carriers: 0

GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 1710
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variant carriers: 0

GenotypeQuality
all individuals: 236
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variant carriers: 0

GenotypeQuality
all individuals: 2039
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variant carriers: 0

GenotypeQuality
all individuals: 1933
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variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1713
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
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variant carriers: 0

GenotypeQuality
all individuals: 931
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variant carriers: 0

GenotypeQuality
all individuals: 1097
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variant carriers: 0

GenotypeQuality
all individuals: 2149
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variant carriers: 0

GenotypeQuality
all individuals: 6527
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variant carriers: 0

GenotypeQuality
all individuals: 517
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variant carriers: 0

GenotypeQuality
all individuals: 1063
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variant carriers: 0

GenotypeQuality
all individuals: 1233
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3725
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65172
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.758583400919168e-5
allele num: 14796
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9616
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.58e0

MQRankSum
type: SiteQuality
SIO_000300: -9.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.837e0

FS
type: SiteQuality
SIO_000300: 5.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.268e0

QD
type: SiteQuality
SIO_000300: 1.182e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e0

DP
type: SiteQuality
SIO_000300: 1.590466e6

GenotypeQuality
all individuals: 847
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 210
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 708
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variant carriers: 0

GenotypeQuality
all individuals: 6539
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variant carriers: 0

GenotypeQuality
all individuals: 709
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GenotypeQuality
all individuals: 505
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variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1557
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 197
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35826
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533224985434363e-5
allele num: 65222
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9620
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14884
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.76e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.342e1

DP
type: SiteQuality
SIO_000300: 1.610447e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.104e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.655e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.35e-1

GenotypeQuality
all individuals: 1763
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
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variant carriers: 0

GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 446
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GenotypeQuality
all individuals: 700
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 3728
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
all individuals: 167
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GenotypeQuality
all individuals: 37845
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GenotypeQuality
all individuals: 1190
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variant carriers: 0

GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 2039
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GenotypeQuality
all individuals: 1129
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
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GenotypeQuality
all individuals: 1686
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GenotypeQuality
all individuals: 6546
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 215
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.590665646518745e-5
allele num: 65350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9660
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

DP
type: SiteQuality
SIO_000300: 1.627356e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.19e-1

QD
type: SiteQuality
SIO_000300: 1.502e1

VQSLOD
type: SiteQuality
SIO_000300: 6.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.87e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
all individuals: 39217
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2052
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GenotypeQuality
all individuals: 6576
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 609
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GenotypeQuality
all individuals: 70
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GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 1690
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GenotypeQuality
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GenotypeQuality
all individuals: 760
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GenotypeQuality
all individuals: 1193
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GenotypeQuality
all individuals: 503
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GenotypeQuality
all individuals: 186
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GenotypeQuality
all individuals: 109
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GenotypeQuality
all individuals: 702
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GenotypeQuality
all individuals: 250
bin: 4.25e1
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GenotypeQuality
all individuals: 1637
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3724
bin: 9.75e1
variant carriers: 2

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

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

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

African
type: Population
allele count: 1
allele frequency: 1.031140441328109e-4
allele num: 9698
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.5253668507276e-5
allele num: 65558
num of homozygotes: 0

ReadPosRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 5.5e-3

FS
type: SiteQuality
SIO_000300: 1.3699e1

QD
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DP
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.946e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.24e-1

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele frequency: 1.518418415378542e-5
allele num: 65858
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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QD
type: SiteQuality
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MQ
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DP
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ReadPosRankSum
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FS
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.35e-1

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.517911353976928e-5
allele num: 65880
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15570
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 9.03e-1

BaseQRankSum
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SIO_000300: 3.91e0

MQ
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SIO_000300: 5.962e1

ReadPosRankSum
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SIO_000300: 6.5e-1

DP
type: SiteQuality
SIO_000300: 1.66199e6

FS
type: SiteQuality
SIO_000300: 8.27e-1

InbreedingCoeff
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SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.94e-1

QD
type: SiteQuality
SIO_000300: 1.167e1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

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

Latino
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allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15570
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65880
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

MQ
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SIO_000300: 5.962e1

InbreedingCoeff
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SIO_000300: 5.0e-4

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 8.27e-1

QD
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DP
type: SiteQuality
SIO_000300: 1.66199e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.03e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15710
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.515840533575868e-5
allele num: 65970
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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East Asian
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.412e0

BaseQRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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SIO_000300: 5.963e1

MQRankSum
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SIO_000300: 2.18e-1

ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9982
num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511852926947267e-5
allele num: 66144
num of homozygotes: 0

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

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

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

South Asian
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num of homozygotes: 0

Other
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European (Finnish)
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num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Non-Finnish)
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African
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East Asian
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 63
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variant carriers: 0

Latino
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allele num: 11540
num of homozygotes: 0

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

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

European (Non-Finnish)
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South Asian
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QD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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DP
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MQ
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FS
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 508
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
all individuals: 3725
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007337904486948e-5
allele num: 66504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.143e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
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SIO_000300: 1.22e0

ClippingRankSum
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SIO_000300: -7.47e-1

FS
type: SiteQuality
SIO_000300: 6.578e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

QD
type: SiteQuality
SIO_000300: 9.960000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.692988e6

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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
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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: 55
bin: 3.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503352476021528e-5
allele num: 66518
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.632e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.693578e6

QD
type: SiteQuality
SIO_000300: 5.12e0

MQRankSum
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SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.13e-1

FS
type: SiteQuality
SIO_000300: 1.229e0

VQSLOD
type: SiteQuality
SIO_000300: -1.638e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 701
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variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
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GenotypeQuality
all individuals: 3721
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

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

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

East Asian
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allele count: 5
allele frequency: 5.780346820809249e-4
allele num: 8650
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

Other
type: Population
allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

BaseQRankSum
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SIO_000300: 3.27e0

VQSLOD
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SIO_000300: 5.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.08e-1

MQRankSum
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SIO_000300: 8.51e-1

FS
type: SiteQuality
SIO_000300: 1.112e0

DP
type: SiteQuality
SIO_000300: 1.695567e6

QD
type: SiteQuality
SIO_000300: 1.492e1

MQ
type: SiteQuality
SIO_000300: 5.92e1

GenotypeDepth
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variant carriers: 1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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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: 38
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variant carriers: 0

GenotypeQuality
all individuals: 43564
bin: 6.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.552e1

VQSLOD
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SIO_000300: 1.17e0

BaseQRankSum
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SIO_000300: 1.72e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 9.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.32e-1

DP
type: SiteQuality
SIO_000300: 1.695193e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 19
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11
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variant carriers: 0

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

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

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

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

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

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

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

African
type: Population
allele count: 0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.581e0

ReadPosRankSum
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SIO_000300: 4.41e-1

MQ
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SIO_000300: 5.964e1

BaseQRankSum
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ClippingRankSum
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QD
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MQRankSum
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SIO_000300: 3.0e-1

InbreedingCoeff
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.698025e6

VQSLOD
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SIO_000300: 2.76e0

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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QD
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ReadPosRankSum
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BaseQRankSum
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MQ
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 1.698059e6

ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3718
bin: 9.75e1
variant carriers: 6

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

African
type: Population
allele count: 3
allele frequency: 2.885170225043277e-4
allele num: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 1.818181818181818e-4
allele num: 16500
num of homozygotes: 0

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

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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MQRankSum
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ClippingRankSum
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MQ
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DP
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QD
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BaseQRankSum
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SIO_000300: 2.58e-1

VQSLOD
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SIO_000300: 4.09e0

InbreedingCoeff
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SIO_000300: -1.0e-4

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 686
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.603486373680334e-5
allele num: 65168
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15600
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

FS
type: SiteQuality
SIO_000300: 1.2486e1

DP
type: SiteQuality
SIO_000300: 1.61211e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

QD
type: SiteQuality
SIO_000300: 1.327e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1138
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 4.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.436663233779608e-5
allele num: 15536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65088
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.155e0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

QD
type: SiteQuality
SIO_000300: 1.452e1

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 6.664e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.567e0

DP
type: SiteQuality
SIO_000300: 1.606573e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15536
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.536381514257621e-5
allele num: 65088
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

FS
type: SiteQuality
SIO_000300: 6.664e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.155e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.567e0

DP
type: SiteQuality
SIO_000300: 1.606573e6

GenotypeQuality
all individuals: 678
bin: 9.25e1
variant carriers: 0

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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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 13

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.016441755855437e-4
allele num: 64470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15314
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 8.53e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

DP
type: SiteQuality
SIO_000300: 1.529043e6

QD
type: SiteQuality
SIO_000300: 1.499e1

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
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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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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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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
all individuals: 22560
bin: 6.25e1
variant carriers: 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: 10050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561231499406732e-5
allele num: 64052
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15044
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

FS
type: SiteQuality
SIO_000300: 2.318e0

DP
type: SiteQuality
SIO_000300: 1.426914e6

QD
type: SiteQuality
SIO_000300: 1.331e1

VQSLOD
type: SiteQuality
SIO_000300: 6.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: -1.655e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 11

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 11
allele frequency: 7.352941176470588e-4
allele num: 14960
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: 10010
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63886
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.393799e6

FS
type: SiteQuality
SIO_000300: 1.113e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 6.042e1

BaseQRankSum
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SIO_000300: 7.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.55e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7240
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.960573476702509e-5
allele num: 11160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8222
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.019386106623587e-4
allele num: 9904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

InbreedingCoeff
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MQ
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.362537379907107e-5
allele num: 62868
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

FS
type: SiteQuality
SIO_000300: 1.909e0

DP
type: SiteQuality
SIO_000300: 1.329402e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.772e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62242
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 1.231223836493475e-4
allele num: 8122
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 3.554e0

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.63e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -5.435e-1

DP
type: SiteQuality
SIO_000300: 1.321226e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.604466835670507e-5
allele num: 62326
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8128
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele count: 12
allele frequency: 1.081860800576993e-3
allele num: 11092
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.320799e6

QD
type: SiteQuality
SIO_000300: 1.236e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

FS
type: SiteQuality
SIO_000300: 3.484e0

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1506
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.81257930034439e-4
allele num: 11034
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8086
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61972
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

MQRankSum
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SIO_000300: -2.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

QD
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SIO_000300: 1.194e1

BaseQRankSum
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ReadPosRankSum
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SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.49e-1

DP
type: SiteQuality
SIO_000300: 1.320111e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 274
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.693820376057325e-5
allele num: 37122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4924
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7494
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MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.69634e5

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

VQSLOD
type: SiteQuality
SIO_000300: -7.066e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 17

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5086
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 4.335628666156592e-4
allele num: 39210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5394
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 7750
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

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

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
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SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

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

Other
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
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African
type: Population
allele count: 1
allele frequency: 1.239771881973717e-4
allele num: 8066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7434
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 41252
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.882e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
type: SiteQuality
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