22-51044276-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044276
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044276
    reference: chr 22
allele count: 1
allele frequency: 2.337978116524829e-5
allele num: 42772
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2035G>C
  hgvsp: ENSP00000330572.3:p.Val679Leu
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1153G>C
  hgvsp: ENSP00000008876.5:p.Val385Leu
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.898G>C
  hgvsp: ENSP00000340015.4:p.Val300Leu
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1204G>C
  hgvsp: ENSP00000404914.2:p.Val402Leu
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1240G>C
  hgvsp: ENSP00000382796.1:p.Val414Leu
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1240G>C
  hgvsp: ENSP00000382792.2:p.Val414Leu
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2183
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2937
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8237
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val679Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

22-51044282-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044282
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044282
    reference: chr 22
allele count: 2
allele frequency: 4.792485382919582e-5
allele num: 41732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1159C>T
  hgvsp: ENSP00000008876.5:p.Arg387Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1246C>T
  hgvsp: ENSP00000382796.1:p.Arg416Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1210C>T
  hgvsp: ENSP00000404914.2:p.Arg404Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2041C>T
  hgvsp: ENSP00000330572.3:p.Arg681Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.904C>T
  hgvsp: ENSP00000340015.4:p.Arg302Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1246C>T
  hgvsp: ENSP00000382792.2:p.Arg416Cys
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9324
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30435
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8363
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg681Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

22-51044283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044283
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044283
    reference: chr 22
allele count: 1
allele frequency: 2.423419930205506e-5
allele num: 41264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1160G>A
  hgvsp: ENSP00000008876.5:p.Arg387His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2042G>A
  hgvsp: ENSP00000330572.3:p.Arg681His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1247G>A
  hgvsp: ENSP00000382792.2:p.Arg416His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1247G>A
  hgvsp: ENSP00000382796.1:p.Arg416His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.905G>A
  hgvsp: ENSP00000340015.4:p.Arg302His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1211G>A
  hgvsp: ENSP00000404914.2:p.Arg404His
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8384
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1838
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 8456
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30317
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg681His
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

22-51044290-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044290
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044290
    reference: chr 22
allele count: 2
allele frequency: 4.895002202750991e-5
allele num: 40858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.912C>T
  hgvsp: ENST00000341339.4:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1218C>T
  hgvsp: ENST00000442429.2:c.1218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1254C>T
  hgvsp: ENST00000399908.2:c.1254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1167C>T
  hgvsp: ENST00000008876.5:c.1167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2049C>T
  hgvsp: ENST00000329492.3:c.2049C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1254C>T
  hgvsp: ENST00000399912.1:c.1254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6101
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8365
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8833
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2970
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31360
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8376
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp683Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

22-51044291-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044291
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044291
    reference: chr 22
allele count: 2
allele frequency: 4.895241824946152e-5
allele num: 40856
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1255G>A
  hgvsp: ENSP00000382796.1:p.Val419Met
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.913G>A
  hgvsp: ENSP00000340015.4:p.Val305Met
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1219G>A
  hgvsp: ENSP00000404914.2:p.Val407Met
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1168G>A
  hgvsp: ENSP00000008876.5:p.Val390Met
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2050G>A
  hgvsp: ENSP00000330572.3:p.Val684Met
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1255G>A
  hgvsp: ENSP00000382792.2:p.Val419Met
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8309
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31013
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8765
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8339
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1847
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32030
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val684Met
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

22-51044308-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044308
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044308
    reference: chr 22
allele count: 1
allele frequency: 2.571884162337328e-5
allele num: 38882
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1236C>T
  hgvsp: ENST00000442429.2:c.1236C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1185C>T
  hgvsp: ENST00000008876.5:c.1185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1272C>T
  hgvsp: ENST00000399912.1:c.1272C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.930C>T
  hgvsp: ENST00000341339.4:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2067C>T
  hgvsp: ENST00000329492.3:c.2067C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1272C>T
  hgvsp: ENST00000399908.2:c.1272C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8856
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32415
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8750
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1140
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser689Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

22-51044309-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044309
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044309
    reference: chr 22
allele count: 2
allele frequency: 5.135579293344289e-5
allele num: 38944
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2068G>A
  hgvsp: ENSP00000330572.3:p.Val690Met
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1273G>A
  hgvsp: ENSP00000382796.1:p.Val425Met
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1237G>A
  hgvsp: ENSP00000404914.2:p.Val413Met
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.931G>A
  hgvsp: ENSP00000340015.4:p.Val311Met
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1186G>A
  hgvsp: ENSP00000008876.5:p.Val396Met
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1273G>A
  hgvsp: ENSP00000382792.2:p.Val425Met
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8805
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33040
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val690Met
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/22-51044333-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044333
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044333
    reference: chr 22
allele count: 1
allele frequency: 2.78473962684489e-5
allele num: 35910
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1261A>C
  hgvsp: ENSP00000404914.2:p.Asn421His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1210A>C
  hgvsp: ENSP00000008876.5:p.Asn404His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2092A>C
  hgvsp: ENSP00000330572.3:p.Asn698His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1297A>C
  hgvsp: ENSP00000382796.1:p.Asn433His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.955A>C
  hgvsp: ENSP00000340015.4:p.Asn319His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1297A>C
  hgvsp: ENSP00000382792.2:p.Asn433His
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11682
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32530
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11693
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn698His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

22-51044335-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044335
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044335
    reference: chr 22
allele count: 10
allele frequency: 2.825018362619357e-4
allele num: 35398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.957C>T
  hgvsp: ENST00000341339.4:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1212C>T
  hgvsp: ENST00000008876.5:c.1212C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1263C>T
  hgvsp: ENST00000442429.2:c.1263C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1299C>T
  hgvsp: ENST00000399912.1:c.1299C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2094C>T
  hgvsp: ENST00000329492.3:c.2094C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1299C>T
  hgvsp: ENST00000399908.2:c.1299C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29699
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12149
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7752
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12189
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn698Asn
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

22-51044336-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044336
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044336
    reference: chr 22
allele count: 1
allele frequency: 2.853229856197215e-5
allele num: 35048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.958G>A
  hgvsp: ENSP00000340015.4:p.Gly320Ser
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2095G>A
  hgvsp: ENSP00000330572.3:p.Gly699Ser
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1300G>A
  hgvsp: ENSP00000382796.1:p.Gly434Ser
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1213G>A
  hgvsp: ENSP00000008876.5:p.Gly405Ser
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1264G>A
  hgvsp: ENSP00000404914.2:p.Gly422Ser
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1300G>A
  hgvsp: ENSP00000382792.2:p.Gly434Ser
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12589
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29422
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2220
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7641
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly699Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

22-51044377-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044377
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044377
    reference: chr 22
allele count: 2
allele frequency: 8.887308922858158e-5
allele num: 22504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1326+15C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1290+15C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1239+15C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.984+15C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2121+15C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1326+15C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15554
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3942
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 925
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29630
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-51044378-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044378
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044378
    reference: chr 22
allele count: 2
allele frequency: 8.952551477170994e-5
allele num: 22340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1290+16G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2121+16G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1326+16G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1326+16G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1239+16G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.984+16G>A
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2586
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1772
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1942
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

22-51044384-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044384
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044384
    reference: chr 22
allele count: 1
allele frequency: 4.837461300309598e-5
allele num: 20672
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1239+22G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1290+22G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.984+22G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2121+22G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1326+22G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1326+22G>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13838
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31303
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3042
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

22-51044386-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044386
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044386
    reference: chr 22
allele count: 1
allele frequency: 4.999000199960008e-5
allele num: 20004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1326+24G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.984+24G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1290+24G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2121+24G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1239+24G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1326+24G>A
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32808
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9802
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31444
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3310
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2418
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

22-51044400-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044400
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044400
    reference: chr 22
allele count: 6
allele frequency: 3.515350363252871e-4
allele num: 17068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.984+38C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1290+38C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1326+38C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2121+38C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1326+38C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1239+38C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11547
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 28159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1454
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2916
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4760
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5817
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

22-51044407-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044407
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044407
    reference: chr 22
allele count: 1284
allele frequency: 7.88988570726312e-2
allele num: 16274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1290+45C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1326+45C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.984+45C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1326+45C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2121+45C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1239+45C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11634
  bin: 7.5e0
  variant carriers: 1157
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 31652
  bin: 2.5e0
  variant carriers: 576
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 3.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 1.75e1
  variant carriers: 354
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 2.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 1.25e1
  variant carriers: 447
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 2.25e1
  variant carriers: 227
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 3.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 3.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 3025
  bin: 1.75e1
  variant carriers: 152
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 4.75e1
  variant carriers: 86
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 2.75e1
  variant carriers: 84
genotype quality: GenotypeQuality
  all individuals: 4323
  bin: 1.25e1
  variant carriers: 121
genotype quality: GenotypeQuality
  all individuals: 24125
  bin: 7.5e0
  variant carriers: 225
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.75e1
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 6.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 8.25e1
  variant carriers: 84
genotype quality: GenotypeQuality
  all individuals: 3840
  bin: 2.25e1
  variant carriers: 257
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 4.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 8478
  bin: 2.5e0
  variant carriers: 10
num of homozygotes: 68
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

22-51044408-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51044408
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51044408
    reference: chr 22
allele count: 2
allele frequency: 1.239618197595141e-4
allele num: 16134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1326+46G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.984+46G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1326+46G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1290+46G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2121+46G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1239+46G>A
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11360
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7535
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3764
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25894
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

22-51045041-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045041
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045041
    reference: chr 22
allele count: 1
allele frequency: 3.738876841396844e-5
allele num: 26746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.985-45T>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2122-45T>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1291-45T>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1240-45T>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1327-45T>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1327-45T>C
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23888
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21865
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11302
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2217
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17477
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2363
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7540
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7425
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

22-51045041-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045041
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045041
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 26746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1291-45T>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1327-45T>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1327-45T>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1240-45T>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2122-45T>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.985-45T>G
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23888
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21865
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7540
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1318
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11302
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2363
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2217
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3769
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

22-51045043-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045043
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045043
    reference: chr 22
allele count: 1
allele frequency: 3.736362277686444e-5
allele num: 26764
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2122-43G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1291-43G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.985-43G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1240-43G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1327-43G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1327-43G>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23591
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12952
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17753
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6180
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3769
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7196
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-51045060-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045060
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045060
    reference: chr 22
allele count: 1
allele frequency: 3.509018176714155e-5
allele num: 28498
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1291-26C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1240-26C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.985-26C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2122-26C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1327-26C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1327-26C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3201
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2638
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14647
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1295
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24581
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

22-51045071-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045071
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045071
    reference: chr 22
allele count: 1
allele frequency: 3.182888789865682e-5
allele num: 31418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1327-15C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1327-15C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1291-15C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1240-15C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2122-15C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.985-15C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11041
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33007
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10353
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3774
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3769
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

22-51045073-ACTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045073
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045070
    reference: chr 22
allele count: 1
allele frequency: 3.1207090250905e-5
allele num: 32044
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2122-7_2122-5delTCT
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1327-7_1327-5delTCT
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.985-7_985-5delTCT
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1240-7_1240-5delTCT
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1327-7_1327-5delTCT
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1291-7_1291-5delTCT
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9621
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1581
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1301
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31359
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: ACTT
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

22-51045077-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045077
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045077
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 33482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1327-9C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1327-9C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1240-9C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2122-9C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.985-9C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1291-9C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34453
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8826
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8363
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1557
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4574
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32952
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

22-51045103-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045103
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045103
    reference: chr 22
allele count: 1
allele frequency: 2.286550509900764e-5
allele num: 43734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1344A>G
  hgvsp: ENST00000399908.2:c.1344A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1308A>G
  hgvsp: ENST00000442429.2:c.1308A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1002A>G
  hgvsp: ENST00000341339.4:c.1002A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1344A>G
  hgvsp: ENST00000399912.1:c.1344A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2139A>G
  hgvsp: ENST00000329492.3:c.2139A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1257A>G
  hgvsp: ENST00000008876.5:c.1257A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34222
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4390
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys713Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

22-51045109-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045109
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045109
    reference: chr 22
allele count: 25
allele frequency: 5.56569749320985e-4
allele num: 44918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1008C>T
  hgvsp: ENST00000341339.4:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1350C>T
  hgvsp: ENST00000399908.2:c.1350C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2145C>T
  hgvsp: ENST00000329492.3:c.2145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1350C>T
  hgvsp: ENST00000399912.1:c.1350C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1314C>T
  hgvsp: ENST00000442429.2:c.1314C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1263C>T
  hgvsp: ENST00000008876.5:c.1263C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 33140
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 33201
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7471
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 5.75e1
  variant carriers: 1
hgvs: p.Thr715Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

22-51045110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045110
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045110
    reference: chr 22
allele count: 1
allele frequency: 2.221333688746724e-5
allele num: 45018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1009G>A
  hgvsp: ENSP00000340015.4:p.Val337Ile
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2146G>A
  hgvsp: ENSP00000330572.3:p.Val716Ile
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1351G>A
  hgvsp: ENSP00000382796.1:p.Val451Ile
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1264G>A
  hgvsp: ENSP00000008876.5:p.Val422Ile
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1315G>A
  hgvsp: ENSP00000404914.2:p.Val439Ile
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1351G>A
  hgvsp: ENSP00000382792.2:p.Val451Ile
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7749
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33353
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val716Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

22-51045110-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045110
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045110
    reference: chr 22
allele count: 2
allele frequency: 4.442667377493447e-5
allele num: 45018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1351G>T
  hgvsp: ENSP00000382796.1:p.Val451Phe
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1009G>T
  hgvsp: ENSP00000340015.4:p.Val337Phe
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1351G>T
  hgvsp: ENSP00000382792.2:p.Val451Phe
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1315G>T
  hgvsp: ENSP00000404914.2:p.Val439Phe
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2146G>T
  hgvsp: ENSP00000330572.3:p.Val716Phe
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1264G>T
  hgvsp: ENSP00000008876.5:p.Val422Phe
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6857
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7749
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33353
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val716Phe
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: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

22-51045116-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045116
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045116
    reference: chr 22
allele count: 1
allele frequency: 2.175710369435621e-5
allele num: 45962
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1357C>T
  hgvsp: ENST00000399908.2:c.1357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2152C>T
  hgvsp: ENST00000329492.3:c.2152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1270C>T
  hgvsp: ENST00000008876.5:c.1270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1015C>T
  hgvsp: ENST00000341339.4:c.1015C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1357C>T
  hgvsp: ENST00000399912.1:c.1357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1321C>T
  hgvsp: ENST00000442429.2:c.1321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2137
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32803
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4412
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6849
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1783
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu718Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

22-51045119-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045119
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045119
    reference: chr 22
allele count: 3
allele frequency: 6.44800756566221e-5
allele num: 46526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1324C>T
  hgvsp: ENSP00000404914.2:p.Arg442Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2155C>T
  hgvsp: ENSP00000330572.3:p.Arg719Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1273C>T
  hgvsp: ENSP00000008876.5:p.Arg425Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1018C>T
  hgvsp: ENSP00000340015.4:p.Arg340Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1360C>T
  hgvsp: ENSP00000382796.1:p.Arg454Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1360C>T
  hgvsp: ENSP00000382792.2:p.Arg454Cys
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4362
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg719Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

22-51045120-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045120
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045120
    reference: chr 22
allele count: 5
allele frequency: 1.068376068376068e-4
allele num: 46800
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1361G>A
  hgvsp: ENSP00000382796.1:p.Arg454His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1274G>A
  hgvsp: ENSP00000008876.5:p.Arg425His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2156G>A
  hgvsp: ENSP00000330572.3:p.Arg719His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1361G>A
  hgvsp: ENSP00000382792.2:p.Arg454His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1019G>A
  hgvsp: ENSP00000340015.4:p.Arg340His
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1325G>A
  hgvsp: ENSP00000404914.2:p.Arg442His
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32169
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6831
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6365
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1557
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1803
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 874
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 6.75e1
  variant carriers: 1
hgvs: p.Arg719His
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

22-51045121-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045121
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045121
    reference: chr 22
allele count: 1
allele frequency: 2.109615628032573e-5
allele num: 47402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1362C>T
  hgvsp: ENST00000399908.2:c.1362C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1275C>T
  hgvsp: ENST00000008876.5:c.1275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2157C>T
  hgvsp: ENST00000329492.3:c.2157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1326C>T
  hgvsp: ENST00000442429.2:c.1326C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1020C>T
  hgvsp: ENST00000341339.4:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1362C>T
  hgvsp: ENST00000399912.1:c.1362C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6872
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7938
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4305
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg719Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/22-51045133-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045133
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045133
    reference: chr 22
allele count: 1
allele frequency: 2.088641964994361e-5
allele num: 47878
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1374C>A
  hgvsp: ENST00000399912.1:c.1374C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1338C>A
  hgvsp: ENST00000442429.2:c.1338C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2169C>A
  hgvsp: ENST00000329492.3:c.2169C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1374C>A
  hgvsp: ENST00000399908.2:c.1374C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1032C>A
  hgvsp: ENST00000341339.4:c.1032C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1287C>A
  hgvsp: ENST00000008876.5:c.1287C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3776
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33142
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6500
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser723Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

22-51045135-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045135
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045135
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 47716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1376G>A
  hgvsp: ENSP00000382792.2:p.Cys459Tyr
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1376G>A
  hgvsp: ENSP00000382796.1:p.Cys459Tyr
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2171G>A
  hgvsp: ENSP00000330572.3:p.Cys724Tyr
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1289G>A
  hgvsp: ENSP00000008876.5:p.Cys430Tyr
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1034G>A
  hgvsp: ENSP00000340015.4:p.Cys345Tyr
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1340G>A
  hgvsp: ENSP00000404914.2:p.Cys447Tyr
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31044
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8747
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3777
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1831
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32602
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Cys724Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

22-51045140-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045140
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045140
    reference: chr 22
allele count: 1
allele frequency: 2.107215104517869e-5
allele num: 47456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1381C>T
  hgvsp: ENSP00000382796.1:p.Leu461Phe
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2176C>T
  hgvsp: ENSP00000330572.3:p.Leu726Phe
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1345C>T
  hgvsp: ENSP00000404914.2:p.Leu449Phe
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1039C>T
  hgvsp: ENSP00000340015.4:p.Leu347Phe
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1294C>T
  hgvsp: ENSP00000008876.5:p.Leu432Phe
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1381C>T
  hgvsp: ENSP00000382792.2:p.Leu461Phe
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3777
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5608
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3016
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2267
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4775
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu726Phe
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

22-51045146-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045146
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045146
    reference: chr 22
allele count: 1
allele frequency: 2.084114876411988e-5
allele num: 47982
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2182A>G
  hgvsp: ENSP00000330572.3:p.Ile728Val
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1387A>G
  hgvsp: ENSP00000382796.1:p.Ile463Val
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1387A>G
  hgvsp: ENSP00000382792.2:p.Ile463Val
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1045A>G
  hgvsp: ENSP00000340015.4:p.Ile349Val
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1300A>G
  hgvsp: ENSP00000008876.5:p.Ile434Val
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1351A>G
  hgvsp: ENSP00000404914.2:p.Ile451Val
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2101
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5865
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile728Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

22-51045155-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045155
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045155
    reference: chr 22
allele count: 4
allele frequency: 8.566044200788077e-5
allele num: 46696
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2191C>T
  hgvsp: ENSP00000330572.3:p.Arg731Trp
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1360C>T
  hgvsp: ENSP00000404914.2:p.Arg454Trp
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1309C>T
  hgvsp: ENSP00000008876.5:p.Arg437Trp
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1054C>T
  hgvsp: ENSP00000340015.4:p.Arg352Trp
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1396C>T
  hgvsp: ENSP00000382792.2:p.Arg466Trp
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1396C>T
  hgvsp: ENSP00000382796.1:p.Arg466Trp
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10479
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2736
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6912
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2572
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2121
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3904
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg731Trp
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

22-51045156-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045156
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045156
    reference: chr 22
allele count: 4
allele frequency: 8.64790072209971e-5
allele num: 46254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1397G>A
  hgvsp: ENSP00000382796.1:p.Arg466Gln
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2192G>A
  hgvsp: ENSP00000330572.3:p.Arg731Gln
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1361G>A
  hgvsp: ENSP00000404914.2:p.Arg454Gln
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1055G>A
  hgvsp: ENSP00000340015.4:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1397G>A
  hgvsp: ENSP00000382792.2:p.Arg466Gln
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1310G>A
  hgvsp: ENSP00000008876.5:p.Arg437Gln
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29298
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10517
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7140
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29354
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2572
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2258
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg731Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

22-51045178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045178
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045178
    reference: chr 22
allele count: 28
allele frequency: 6.310570205093532e-4
allele num: 44370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1332C>T
  hgvsp: ENST00000008876.5:c.1332C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1077C>T
  hgvsp: ENST00000341339.4:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1419C>T
  hgvsp: ENST00000399912.1:c.1419C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1383C>T
  hgvsp: ENST00000442429.2:c.1383C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2214C>T
  hgvsp: ENST00000329492.3:c.2214C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1419C>T
  hgvsp: ENST00000399908.2:c.1419C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10268
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28926
  bin: 7.5e0
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4030
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4676
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23858
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2657
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9006
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.75e1
  variant carriers: 2
hgvs: p.Ser738Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

22-51045179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045179
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045179
    reference: chr 22
allele count: 2
allele frequency: 4.47267197423741e-5
allele num: 44716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1420G>A
  hgvsp: ENSP00000382796.1:p.Gly474Arg
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1078G>A
  hgvsp: ENSP00000340015.4:p.Gly360Arg
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1333G>A
  hgvsp: ENSP00000008876.5:p.Gly445Arg
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1384G>A
  hgvsp: ENSP00000404914.2:p.Gly462Arg
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2215G>A
  hgvsp: ENSP00000330572.3:p.Gly739Arg
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1420G>A
  hgvsp: ENSP00000382792.2:p.Gly474Arg
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2635
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3907
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2688
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3821
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24922
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2857
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly739Arg
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

22-51045184-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045184
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045184
    reference: chr 22
allele count: 1
allele frequency: 2.268911376321641e-5
allele num: 44074
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1425A>G
  hgvsp: ENST00000399912.1:c.1425A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1338A>G
  hgvsp: ENST00000008876.5:c.1338A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1083A>G
  hgvsp: ENST00000341339.4:c.1083A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1389A>G
  hgvsp: ENST00000442429.2:c.1389A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2220A>G
  hgvsp: ENST00000329492.3:c.2220A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1425A>G
  hgvsp: ENST00000399908.2:c.1425A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7787
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1458
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3776
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9006
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6009
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly740Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

22-51045185-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045185
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045185
    reference: chr 22
allele count: 1
allele frequency: 2.270972430394695e-5
allele num: 44034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1084G>A
  hgvsp: ENSP00000340015.4:p.Gly362Arg
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1426G>A
  hgvsp: ENSP00000382792.2:p.Gly476Arg
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2221G>A
  hgvsp: ENSP00000330572.3:p.Gly741Arg
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1339G>A
  hgvsp: ENSP00000008876.5:p.Gly447Arg
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1390G>A
  hgvsp: ENSP00000404914.2:p.Gly464Arg
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1426G>A
  hgvsp: ENSP00000382796.1:p.Gly476Arg
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7744
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6364
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8948
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4453
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly741Arg
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

22-51045187-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045187
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045187
    reference: chr 22
allele count: 10
allele frequency: 2.388915432393693e-4
allele num: 41860
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1341G>T
  hgvsp: ENST00000008876.5:c.1341G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1428G>T
  hgvsp: ENST00000399908.2:c.1428G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1086G>T
  hgvsp: ENST00000341339.4:c.1086G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1428G>T
  hgvsp: ENST00000399912.1:c.1428G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2223G>T
  hgvsp: ENST00000329492.3:c.2223G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1392G>T
  hgvsp: ENST00000442429.2:c.1392G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10938
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28490
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7555
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4854
  bin: 1.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2760
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 18815
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2956
  bin: 2.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3709
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 4.75e1
  variant carriers: 2
hgvs: p.Gly741Gly
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

22-51045190-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045190
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045190
    reference: chr 22
allele count: 36512
allele frequency: 6.447921449510825e-1
allele num: 56626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1089C>T
  hgvsp: ENST00000341339.4:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1431C>T
  hgvsp: ENST00000399908.2:c.1431C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2226C>T
  hgvsp: ENST00000329492.3:c.2226C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1395C>T
  hgvsp: ENST00000442429.2:c.1395C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1344C>T
  hgvsp: ENST00000008876.5:c.1344C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1431C>T
  hgvsp: ENST00000399912.1:c.1431C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.25e1
  variant carriers: 647
genotype depth: GenotypeDepth
  all individuals: 4702
  bin: 2.5e0
  variant carriers: 2214
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.75e1
  variant carriers: 511
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 1.75e1
  variant carriers: 4045
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.25e1
  variant carriers: 763
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 2.25e1
  variant carriers: 1223
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 5.75e1
  variant carriers: 683
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 2.75e1
  variant carriers: 657
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 174
genotype depth: GenotypeDepth
  all individuals: 23824
  bin: 7.5e0
  variant carriers: 16785
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 699
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 568
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.25e1
  variant carriers: 774
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.25e1
  variant carriers: 332
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 247
genotype depth: GenotypeDepth
  all individuals: 15330
  bin: 1.25e1
  variant carriers: 13111
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.75e1
  variant carriers: 810
genotype quality: GenotypeQuality
  all individuals: 17003
  bin: 9.75e1
  variant carriers: 16843
genotype quality: GenotypeQuality
  all individuals: 2842
  bin: 7.5e0
  variant carriers: 1007
genotype quality: GenotypeQuality
  all individuals: 4982
  bin: 2.5e0
  variant carriers: 222
genotype quality: GenotypeQuality
  all individuals: 2101
  bin: 1.25e1
  variant carriers: 1488
genotype quality: GenotypeQuality
  all individuals: 4592
  bin: 1.75e1
  variant carriers: 4014
genotype quality: GenotypeQuality
  all individuals: 7832
  bin: 2.25e1
  variant carriers: 4324
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 5.75e1
  variant carriers: 676
genotype quality: GenotypeQuality
  all individuals: 3539
  bin: 3.25e1
  variant carriers: 3228
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 8.75e1
  variant carriers: 1084
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 1280
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 8.25e1
  variant carriers: 933
hgvs: p.Pro742Pro
num of homozygotes: 11322
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

22-51045191-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045191
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045191
    reference: chr 22
allele count: 1
allele frequency: 2.033098849266051e-5
allele num: 49186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1345G>A
  hgvsp: ENSP00000008876.5:p.Glu449Lys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1090G>A
  hgvsp: ENSP00000340015.4:p.Glu364Lys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1432G>A
  hgvsp: ENSP00000382796.1:p.Glu478Lys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2227G>A
  hgvsp: ENSP00000330572.3:p.Glu743Lys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1432G>A
  hgvsp: ENSP00000382792.2:p.Glu478Lys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1396G>A
  hgvsp: ENSP00000404914.2:p.Glu466Lys
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13620
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3589
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4226
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5320
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9824
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu743Lys
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

22-51045196-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045196
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045196
    reference: chr 22
allele count: 1
allele frequency: 2.132105240714682e-5
allele num: 46902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+3G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+3G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+3G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+3G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+3G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+3G>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12778
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10012
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1563
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5051
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3086
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10420
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6158
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18778
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 8.25e1
  variant carriers: 0
hgvs: c.2229+3G>T
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

22-51045202-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045202
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045202
    reference: chr 22
allele count: 47
allele frequency: 1.006682659355723e-3
allele num: 46688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+9G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+9G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+9G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+9G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+9G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+9G>A
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25702
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12593
  bin: 1.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4772
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3625
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10613
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3165
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 20231
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5019
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3574
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

22-51045204-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045204
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045204
    reference: chr 22
allele count: 1
allele frequency: 2.178554311358982e-5
allele num: 45902
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+11G>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+11G>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+11G>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+11G>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+11G>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+11G>C
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3574
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10613
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3581
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5477
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19270
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5195
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

22-51045207-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045207
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045207
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 46064
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+14G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+14G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+14G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+14G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+14G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+14G>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25966
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19984
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4966
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5078
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10624
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3622
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3592
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

22-51045215-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045215
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045215
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 47020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+22G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+22G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+22G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+22G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+22G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+22G>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26472
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3865
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9782
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4015
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22704
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3730
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

22-51045218-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045218
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045218
    reference: chr 22
allele count: 1
allele frequency: 2.122421258171322e-5
allele num: 47116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+25C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+25C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+25C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+25C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+25C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+25C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12975
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3753
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3434
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3327
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1581
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9032
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3295
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

22-51045219-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045219
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045219
    reference: chr 22
allele count: 5
allele frequency: 1.057932376962465e-4
allele num: 47262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+26G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+26G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+26G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+26G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+26G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+26G>A
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7983
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13035
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3924
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3745
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3176
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1651
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1750
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3132
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

22-51045219-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045219
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045219
    reference: chr 22
allele count: 2
allele frequency: 4.231729507849858e-5
allele num: 47262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+26G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+26G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+26G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+26G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+26G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+26G>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7983
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13035
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8512
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3132
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3924
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3802
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23966
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1750
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

22-51045224-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045224
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045224
    reference: chr 22
allele count: 1
allele frequency: 1.982553528945282e-5
allele num: 50440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+31C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+31C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+31C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+31C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+31C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+31C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13164
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3902
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6926
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4403
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2055
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3990
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

22-51045226-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045226
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045226
    reference: chr 22
allele count: 11
allele frequency: 2.148941158083926e-4
allele num: 51188
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+33G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+33G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+33G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+33G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+33G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+33G>A
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27908
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5663
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13031
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3814
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3906
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1759
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4797
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6074
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28932
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

22-51045228-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045228
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045228
    reference: chr 22
allele count: 2
allele frequency: 3.80300437345503e-5
allele num: 52590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+35G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+35G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+35G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+35G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+35G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+35G>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12924
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27938
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3809
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3924
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29437
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1514
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1436
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5516
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

22-51045230-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045230
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045230
    reference: chr 22
allele count: 3098
allele frequency: 5.556751327306644e-2
allele num: 55752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+37G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+37G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+37G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+37G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+37G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+37G>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 2.25e1
  variant carriers: 379
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 1.75e1
  variant carriers: 808
genotype depth: GenotypeDepth
  all individuals: 13256
  bin: 1.25e1
  variant carriers: 1314
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 2.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 2.75e1
  variant carriers: 130
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 26798
  bin: 7.5e0
  variant carriers: 710
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 4065
  bin: 9.75e1
  variant carriers: 2789
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 6.75e1
  variant carriers: 72
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 9.25e1
  variant carriers: 104
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 7.75e1
  variant carriers: 88
genotype quality: GenotypeQuality
  all individuals: 27149
  bin: 2.25e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 1.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 4694
  bin: 7.5e0
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 5.25e1
  variant carriers: 49
genotype quality: GenotypeQuality
  all individuals: 3635
  bin: 3.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 4.75e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 4.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 3509
  bin: 2.75e1
  variant carriers: 30
num of homozygotes: 94
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

22-51045233-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045233
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045233
    reference: chr 22
allele count: 1
allele frequency: 1.72962501729625e-5
allele num: 57816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+40A>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+40A>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+40A>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+40A>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+40A>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+40A>G
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6648
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3777
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28278
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3958
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2385
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4170
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

22-51045235-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045235
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045235
    reference: chr 22
allele count: 1
allele frequency: 1.687592817604968e-5
allele num: 59256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+42G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+42G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+42G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+42G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+42G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+42G>A
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3534
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4154
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3730
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1267
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

22-51045236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045236
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045236
    reference: chr 22
allele count: 1
allele frequency: 1.671793500066872e-5
allele num: 59816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1347+43G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1092+43G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1434+43G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1398+43G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1434+43G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2229+43G>A
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12673
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7354
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27881
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3365
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7065
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3711
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

22-51045302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045302
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045302
    reference: chr 22
allele count: 15
allele frequency: 1.251606227992591e-4
allele num: 119846
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-47C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-47C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-47C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-47C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-47C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-47C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8873
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6383
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3892
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3395
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3497
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2568
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

22-51045303-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045303
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045303
    reference: chr 22
allele count: 6
allele frequency: 5.005088506648426e-5
allele num: 119878
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-46G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-46G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-46G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-46G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-46G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-46G>A
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6889
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9013
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3487
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5888
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2596
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

22-51045307-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045307
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045307
    reference: chr 22
allele count: 2
allele frequency: 1.666638889351844e-5
allele num: 120002
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-42G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-42G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-42G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-42G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-42G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-42G>A
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9182
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8086
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2457
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3580
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4080
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3461
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

22-51045308-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045308
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045308
    reference: chr 22
allele count: 2
allele frequency: 1.666527789350887e-5
allele num: 120010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-41G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-41G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-41G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-41G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-41G>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-41G>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9063
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32319
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3552
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6626
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

22-51045315-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045315
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045315
    reference: chr 22
allele count: 1
allele frequency: 8.325840077263796e-6
allele num: 120108
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-34T>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-34T>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-34T>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-34T>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-34T>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-34T>C
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7039
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2670
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3604
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3587
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2471
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/22-51045320-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045320
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045320
    reference: chr 22
allele count: 2
allele frequency: 1.664752201634787e-5
allele num: 120138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-29A>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-29A>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-29A>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-29A>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-29A>C
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-29A>C
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2682
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3471
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3599
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3614
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

22-51045330-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045330
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045330
    reference: chr 22
allele count: 1
allele frequency: 8.3166999334664e-6
allele num: 120240
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-19C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-19C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-19C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-19C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-19C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-19C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3615
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4193
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32358
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3475
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2697
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
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: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

22-51045332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045332
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045332
    reference: chr 22
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-17G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-17G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-17G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-17G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-17G>A
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-17G>A
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2697
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3475
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32358
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4194
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3614
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum

22-51045335-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045335
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045335
    reference: chr 22
allele count: 1
allele frequency: 8.313242996092776e-6
allele num: 120290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-14C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-14C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-14C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-14C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-14C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-14C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7320
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2704
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genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 2481
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3629
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

22-51045337-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045337
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045337
    reference: chr 22
allele count: 1
allele frequency: 8.31282835672009e-6
allele num: 120296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-12C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-12C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-12C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-12C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-12C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-12C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6406
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4223
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3627
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2709
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3616
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2479
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7354
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

22-51045340-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045340
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045340
    reference: chr 22
allele count: 1
allele frequency: 8.311308366163002e-6
allele num: 120318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-9C>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-9C>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-9C>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-9C>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-9C>G
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-9C>G
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32367
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7379
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3625
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3616
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4235
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2711
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

22-51045345-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045345
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045345
    reference: chr 22
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1435-4C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1093-4C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2230-4C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1435-4C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1348-4C>T
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1399-4C>T
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6406
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32366
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7404
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2710
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
hgvs: c.2230-4C>T
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

22-51045355-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51045355
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 51045355
    reference: chr 22
allele count: 404
allele frequency: 3.35631801944006e-3
allele num: 120370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382796
  ensembl transcript: ENST00000399912
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399912.1:c.1441C>T
  hgvsp: ENSP00000382796.1:p.Arg481Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000404914
  ensembl transcript: ENST00000442429
  gene symbol: MAPK8IP2
  hgvsc: ENST00000442429.2:c.1405C>T
  hgvsp: ENSP00000404914.2:p.Arg469Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000008876
  ensembl transcript: ENST00000008876
  gene symbol: MAPK8IP2
  hgvsc: ENST00000008876.5:c.1354C>T
  hgvsp: ENSP00000008876.5:p.Arg452Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000340015
  ensembl transcript: ENST00000341339
  gene symbol: MAPK8IP2
  hgvsc: ENST00000341339.4:c.1099C>T
  hgvsp: ENSP00000340015.4:p.Arg367Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000382792
  ensembl transcript: ENST00000399908
  gene symbol: MAPK8IP2
  hgvsc: ENST00000399908.2:c.1441C>T
  hgvsp: ENSP00000382792.2:p.Arg481Cys
  variant of: http://identifiers.org/hgnc/6883
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008735
  ensembl protein: ENSP00000330572
  ensembl transcript: ENST00000329492
  gene symbol: MAPK8IP2
  hgvsc: ENST00000329492.3:c.2236C>T
  hgvsp: ENSP00000330572.3:p.Arg746Cys
  variant of: http://identifiers.org/hgnc/6883
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 6.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9084
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9364
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7325
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6383
  bin: 4.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 9.75e1
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 4.25e1
  variant carriers: 7
hgvs: p.Arg746Cys
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 268
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30834
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8541
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.292582417582418e-5
allele num: 23296
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9216
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2220
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.513e0

VQSLOD
type: SiteQuality
SIO_000300: 5.09e-1

DP
type: SiteQuality
SIO_000300: 6.48535e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.65e-2

QD
type: SiteQuality
SIO_000300: 1.246e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

GenotypeQuality
all individuals: 1864
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3013
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 30725
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8555
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 8.831581736288969e-5
allele num: 22646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9196
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.95e-2

FS
type: SiteQuality
SIO_000300: 1.331e0

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

DP
type: SiteQuality
SIO_000300: 6.46197e5

GenotypeQuality
all individuals: 663
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 112
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variant carriers: 1

GenotypeQuality
all individuals: 997
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.463488662738796e-5
allele num: 22404
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-2

QD
type: SiteQuality
SIO_000300: 1.024e1

VQSLOD
type: SiteQuality
SIO_000300: 2.15e0

DP
type: SiteQuality
SIO_000300: 6.44821e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.01e-2

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 8634
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2090
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 9.026900162484202e-5
allele num: 22156
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.96e-2

DP
type: SiteQuality
SIO_000300: 6.44196e5

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.131e1

GenotypeQuality
all individuals: 585
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variant carriers: 0

GenotypeQuality
all individuals: 2505
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 985
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variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 9.035872413481521e-5
allele num: 22134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2108
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.211e1

VQSLOD
type: SiteQuality
SIO_000300: 6.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 1.237e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.95e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
type: SiteQuality
SIO_000300: 6.45336e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 220
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
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GenotypeQuality
all individuals: 207
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1184
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.767807761991036e-5
allele num: 20974
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.035e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.296e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.04e-2

QD
type: SiteQuality
SIO_000300: 4.77e0

DP
type: SiteQuality
SIO_000300: 6.35295e5

GenotypeQuality
all individuals: 2189
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 1

GenotypeQuality
all individuals: 495
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GenotypeQuality
all individuals: 1486
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variant carriers: 0

GenotypeQuality
all individuals: 8728
bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 207
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variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 5.01002004008016e-4
allele num: 1996
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.986857825567503e-4
allele num: 3348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8950
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2152
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.386e0

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 4.702e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.02e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.153e0

VQSLOD
type: SiteQuality
SIO_000300: -2.215e0

DP
type: SiteQuality
SIO_000300: 6.36024e5

QD
type: SiteQuality
SIO_000300: 5.62e0

MQ
type: SiteQuality
SIO_000300: 5.811e1

GenotypeQuality
all individuals: 822
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 251
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variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 355
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variant carriers: 0

GenotypeQuality
all individuals: 147
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GenotypeQuality
all individuals: 111
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variant carriers: 1

GenotypeQuality
all individuals: 7946
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.236150382238978e-5
allele num: 19098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1978
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.41e-2

QD
type: SiteQuality
SIO_000300: 1.012e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.01684e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.65e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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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
all individuals: 93
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.246753246753247e-4
allele num: 3080
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.297266253158741e-4
allele num: 8706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
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East Asian
type: Population
allele count: 3
allele frequency: 1.544799176107106e-3
allele num: 1942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 2.127659574468085e-4
allele num: 18800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1746
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.028e1

FS
type: SiteQuality
SIO_000300: 5.668e0

DP
type: SiteQuality
SIO_000300: 5.97387e5

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 31478
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GenotypeQuality
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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: 100
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GenotypeQuality
all individuals: 243
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.241090146750524e-4
allele num: 1908
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1708
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3064
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.59e-2

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.92554e5

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-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
all individuals: 110
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variant carriers: 2

GenotypeQuality
all individuals: 159
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.230201218386561e-5
allele num: 10834
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.316829075585989e-4
allele num: 7594
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2116
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 252
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
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VQSLOD
type: SiteQuality
SIO_000300: -1.036e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.84e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.552e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.08166e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.28e-1

GenotypeQuality
all individuals: 29830
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GenotypeQuality
all individuals: 13398
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 566
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GenotypeQuality
all individuals: 4043
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GenotypeQuality
all individuals: 155
bin: 7.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.342301943198804e-5
allele num: 10704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2094
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.319261213720317e-4
allele num: 7580
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.386e1

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.88e-2

FS
type: SiteQuality
SIO_000300: 2.074e0

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 4.07053e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

GenotypeQuality
all individuals: 108
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11106
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3499
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2020
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.337971635001338e-4
allele num: 7474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.16e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.284e1

DP
type: SiteQuality
SIO_000300: 3.78706e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.777e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

GenotypeQuality
all individuals: 621
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1872
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7396
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 5.117707267144319e-4
allele num: 1954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9092
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.67218e5

QD
type: SiteQuality
SIO_000300: 1.478e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.069e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.34e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e0

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

GenotypeQuality
all individuals: 259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4955
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 6
allele frequency: 8.588605782994561e-4
allele num: 6986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

FS
type: SiteQuality
SIO_000300: 6.341e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.92e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

DP
type: SiteQuality
SIO_000300: 3.13656e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.352e1

GenotypeQuality
all individuals: 183
bin: 5.75e1
variant carriers: 132

GenotypeQuality
all individuals: 159
bin: 8.75e1
variant carriers: 142

GenotypeQuality
all individuals: 451
bin: 5.25e1
variant carriers: 150

GenotypeQuality
all individuals: 1282
bin: 3.25e1
variant carriers: 30

GenotypeQuality
all individuals: 819
bin: 6.25e1
variant carriers: 39

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 101

GenotypeQuality
all individuals: 1261
bin: 9.75e1
variant carriers: 1180

East Asian
type: Population
allele count: 2
allele frequency: 3.92156862745098e-3
allele num: 510
num of homozygotes: 0

African
type: Population
allele count: 103
allele frequency: 6.204819277108434e-2
allele num: 1660
num of homozygotes: 3

South Asian
type: Population
allele count: 558
allele frequency: 8.398555087296809e-2
allele num: 6644
num of homozygotes: 34

Other
type: Population
allele count: 12
allele frequency: 7.5e-2
allele num: 160
num of homozygotes: 0

Latino
type: Population
allele count: 17
allele frequency: 4.857142857142857e-2
allele num: 350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 13
allele frequency: 1.585365853658537e-1
allele num: 82
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 579
allele frequency: 8.430401863715783e-2
allele num: 6868
num of homozygotes: 30

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.25e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.07942e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

QD
type: SiteQuality
SIO_000300: 1.645e1

GenotypeQuality
all individuals: 3865
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1003
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5025
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6760
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.906976744186046e-3
allele num: 344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6656
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 6.172839506172839e-4
allele num: 1620
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.03739e5

QD
type: SiteQuality
SIO_000300: 1.331e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.03e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

GenotypeQuality
all individuals: 1164
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3769
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 382
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1052
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2622
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.18e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

VQSLOD
type: SiteQuality
SIO_000300: -1.568e0

QD
type: SiteQuality
SIO_000300: 1.109e1

DP
type: SiteQuality
SIO_000300: 6.29571e5

GenotypeQuality
all individuals: 17477
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7425
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1052
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.109e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.568e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.18e-2

DP
type: SiteQuality
SIO_000300: 6.29571e5

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.89e-1

GenotypeQuality
all individuals: 175
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2464
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.241310824230387e-4
allele num: 8056
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1050
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.045e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.69e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.57e-1

DP
type: SiteQuality
SIO_000300: 6.34159e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3773
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 9.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.590708972218005e-5
allele num: 13174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 924
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8184
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1246
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2772
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.45e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.407e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 1.156e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

DP
type: SiteQuality
SIO_000300: 6.88677e5

GenotypeQuality
all individuals: 566
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 217
bin: 4.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2018
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3038
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.547008547008547e-4
allele num: 1170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1582
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.588e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.16e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.8e-2

FS
type: SiteQuality
SIO_000300: 6.994e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 7.34465e5

GenotypeQuality
all individuals: 3773
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4000
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
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GenotypeQuality
all individuals: 89
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GenotypeQuality
all individuals: 382
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variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.195600191296031e-4
allele num: 8364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1672
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2044
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.266e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 5.79e1

FS
type: SiteQuality
SIO_000300: 4.789e0

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 7.41859e5

GenotypeQuality
all individuals: 222
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1336
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3194
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.58508e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.75e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.415e-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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variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9000
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2808
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.395604395604395e-5
allele num: 22750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-2

DP
type: SiteQuality
SIO_000300: 8.46476e5

QD
type: SiteQuality
SIO_000300: 2.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e0

MQ
type: SiteQuality
SIO_000300: 5.875e1

VQSLOD
type: SiteQuality
SIO_000300: -4.337e0

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

FS
type: SiteQuality
SIO_000300: 2.187e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e0

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: 3

GenotypeQuality
all individuals: 3792
bin: 9.75e1
variant carriers: 23

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2482
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.5e-3
allele num: 400
num of homozygotes: 0

South Asian
type: Population
allele count: 16
allele frequency: 1.762114537444934e-3
allele num: 9080
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2916
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 8.116883116883117e-4
allele num: 2464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 2.551020408163266e-4
allele num: 23520
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

DP
type: SiteQuality
SIO_000300: 8.51618e5

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-1

FS
type: SiteQuality
SIO_000300: 1.108e0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

QD
type: SiteQuality
SIO_000300: 1.102e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3776
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2952
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9078
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4066
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.240162822252374e-5
allele num: 23584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2474
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.38e-1

DP
type: SiteQuality
SIO_000300: 8.53256e5

VQSLOD
type: SiteQuality
SIO_000300: 2.95e-1

QD
type: SiteQuality
SIO_000300: 7.15e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3776
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 584
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2952
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.918839153959665e-4
allele num: 4066
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23584
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.15e0

VQSLOD
type: SiteQuality
SIO_000300: 2.95e-1

DP
type: SiteQuality
SIO_000300: 8.53256e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.38e-1

GenotypeQuality
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bin: 6.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3775
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GenotypeQuality
all individuals: 571
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3066
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4118
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.092896174863388e-4
allele num: 9150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24154
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.401e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

QD
type: SiteQuality
SIO_000300: 1.821e1

DP
type: SiteQuality
SIO_000300: 8.51676e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

FS
type: SiteQuality
SIO_000300: 2.781e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.07e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 201
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3777
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.083299305839118e-5
allele num: 24490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3118
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.41196333815726e-4
allele num: 4146
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.837298541826554e-4
allele num: 2606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9200
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

FS
type: SiteQuality
SIO_000300: 7.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.224e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

DP
type: SiteQuality
SIO_000300: 8.5689e5

MQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.15e-2

QD
type: SiteQuality
SIO_000300: 9.98e0

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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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 382
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.084363478638039e-4
allele num: 9222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.621796951021732e-4
allele num: 24664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4170
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.031e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.58e-1

DP
type: SiteQuality
SIO_000300: 8.56886e5

FS
type: SiteQuality
SIO_000300: 2.657e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.79e-1

GenotypeQuality
all individuals: 572
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 518
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GenotypeQuality
all individuals: 1253
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.997122072108082e-5
allele num: 25018
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.332e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

DP
type: SiteQuality
SIO_000300: 8.58751e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.88e-1

QD
type: SiteQuality
SIO_000300: 1.292e1

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
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GenotypeQuality
all individuals: 4890
bin: 7.5e0
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GenotypeQuality
all individuals: 569
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GenotypeQuality
all individuals: 1589
bin: 1.75e1
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GenotypeQuality
all individuals: 382
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GenotypeQuality
all individuals: 1753
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GenotypeQuality
all individuals: 1049
bin: 6.75e1
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GenotypeQuality
all individuals: 570
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4256
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.103662321539416e-4
allele num: 3222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2678
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

DP
type: SiteQuality
SIO_000300: 8.46816e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.287e0

FS
type: SiteQuality
SIO_000300: 3.392e0

QD
type: SiteQuality
SIO_000300: 1.219e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.086e0

GenotypeQuality
all individuals: 2022
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5111
bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5883
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3228
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.683e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.26e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.449e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

DP
type: SiteQuality
SIO_000300: 8.41263e5

QD
type: SiteQuality
SIO_000300: 8.43e0

GenotypeQuality
all individuals: 570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.992972368631209e-5
allele num: 25044
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2658
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.691e0

QD
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -1.857e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.24e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.396e0

DP
type: SiteQuality
SIO_000300: 8.31204e5

ClippingRankSum
type: SiteQuality
SIO_000300: 4.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

GenotypeQuality
all individuals: 2080
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3777
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2413
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.932363350373575e-5
allele num: 25430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2706
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3216
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.24133e5

VQSLOD
type: SiteQuality
SIO_000300: -2.255e0

MQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

GenotypeQuality
all individuals: 3779
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 566
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29875
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 986
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 3.261578604044357e-4
allele num: 3066
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4158
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.061738424045491e-5
allele num: 24620
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 7.763975155279503e-4
allele num: 2576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.77e-1

FS
type: SiteQuality
SIO_000300: 8.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.72e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 8.07238e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

QD
type: SiteQuality
SIO_000300: 1.133e1

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 198
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2297
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3777
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3785
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 419
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.367003367003367e-4
allele num: 2970
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2550
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.930817610062893e-4
allele num: 2544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.10475330432641e-5
allele num: 24362
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.075268817204301e-4
allele num: 9300
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.859e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 3.215e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.83e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -9.0e-2

DP
type: SiteQuality
SIO_000300: 8.0435e5

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2481
bin: 6.25e1
variant carriers: 2

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

GenotypeQuality
all individuals: 818
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 146
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variant carriers: 4

GenotypeQuality
all individuals: 990
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GenotypeQuality
all individuals: 557
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GenotypeQuality
all individuals: 3797
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variant carriers: 27

GenotypeQuality
all individuals: 548
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variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.236944324557618e-4
allele num: 9268
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 4.30416068866571e-3
allele num: 2788
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 1.788451711803781e-3
allele num: 3914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 8.592541673827119e-5
allele num: 23276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 1.636661211129296e-3
allele num: 2444
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2302
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.70164e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.02e-2

QD
type: SiteQuality
SIO_000300: 1.257e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.874e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

GenotypeQuality
all individuals: 821
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 547
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 8984
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GenotypeQuality
all individuals: 516
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GenotypeQuality
all individuals: 318
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GenotypeQuality
all individuals: 557
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GenotypeQuality
all individuals: 407
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GenotypeQuality
all individuals: 3777
bin: 9.75e1
variant carriers: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.264392324093817e-5
allele num: 23450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3944
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.076194575979337e-4
allele num: 9292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2446
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 1.35e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

FS
type: SiteQuality
SIO_000300: 1.028e0

DP
type: SiteQuality
SIO_000300: 7.71211e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 514
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 806
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GenotypeQuality
all individuals: 4439
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variant carriers: 0

GenotypeQuality
all individuals: 555
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GenotypeQuality
all individuals: 379
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GenotypeQuality
all individuals: 1965
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variant carriers: 0

GenotypeQuality
all individuals: 21987
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 2928
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.338771259979174e-5
allele num: 23048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e0

VQSLOD
type: SiteQuality
SIO_000300: -5.663e-1

FS
type: SiteQuality
SIO_000300: 2.933e0

QD
type: SiteQuality
SIO_000300: 8.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

MQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.67542e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.89e-2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1478
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GenotypeQuality
all individuals: 1902
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GenotypeQuality
all individuals: 556
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GenotypeQuality
all individuals: 756
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GenotypeQuality
all individuals: 78
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GenotypeQuality
all individuals: 2952
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2764
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2332
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.079680414597279e-4
allele num: 9262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22990
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.89e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.421e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.019e1

FS
type: SiteQuality
SIO_000300: 8.987e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 7.67817e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

GenotypeQuality
all individuals: 1449
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
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GenotypeQuality
all individuals: 1631
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8838
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GenotypeQuality
all individuals: 380
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GenotypeQuality
all individuals: 372
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GenotypeQuality
all individuals: 530
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GenotypeQuality
all individuals: 499
bin: 9.25e1
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GenotypeQuality
all individuals: 7199
bin: 1.75e1
variant carriers: 3

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9196
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 2.290426019239579e-4
allele num: 21830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2246
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 9.478672985781991e-4
allele num: 2110
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 1.221498371335505e-3
allele num: 2456
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.391e0

QD
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 4.7618e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.67e-2

DP
type: SiteQuality
SIO_000300: 7.7128e5

VQSLOD
type: SiteQuality
SIO_000300: -1.109e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

GenotypeQuality
all individuals: 929
bin: 4.25e1
variant carriers: 893

GenotypeQuality
all individuals: 714
bin: 6.75e1
variant carriers: 492

GenotypeQuality
all individuals: 1001
bin: 5.25e1
variant carriers: 975

GenotypeQuality
all individuals: 803
bin: 7.75e1
variant carriers: 722

GenotypeQuality
all individuals: 2550
bin: 2.75e1
variant carriers: 2149

GenotypeQuality
all individuals: 542
bin: 7.25e1
variant carriers: 453

GenotypeQuality
all individuals: 2381
bin: 3.75e1
variant carriers: 2224

GenotypeQuality
all individuals: 1250
bin: 6.25e1
variant carriers: 578

GenotypeQuality
all individuals: 1096
bin: 9.25e1
variant carriers: 1060

European (Non-Finnish)
type: Population
allele count: 20170
allele frequency: 6.527930610395495e-1
allele num: 30898
num of homozygotes: 6170

Latino
type: Population
allele count: 2217
allele frequency: 6.269796380090498e-1
allele num: 3536
num of homozygotes: 627

East Asian
type: Population
allele count: 2996
allele frequency: 8.159041394335512e-1
allele num: 3672
num of homozygotes: 1205

South Asian
type: Population
allele count: 6891
allele frequency: 6.463140123804164e-1
allele num: 10662
num of homozygotes: 2200

African
type: Population
allele count: 2047
allele frequency: 4.554962171784602e-1
allele num: 4494
num of homozygotes: 429

European (Finnish)
type: Population
allele count: 1894
allele frequency: 6.517549896765313e-1
allele num: 2906
num of homozygotes: 601

Other
type: Population
allele count: 297
allele frequency: 6.48471615720524e-1
allele num: 458
num of homozygotes: 90

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.263e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.46e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

DP
type: SiteQuality
SIO_000300: 8.93911e5

VQSLOD
type: SiteQuality
SIO_000300: 6.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 5.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

GenotypeQuality
all individuals: 352
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3585
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 327
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2758
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4022
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.786157807057398e-5
allele num: 26412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2586
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

QD
type: SiteQuality
SIO_000300: 9.81e0

VQSLOD
type: SiteQuality
SIO_000300: 2.83e-1

DP
type: SiteQuality
SIO_000300: 7.10145e5

FS
type: SiteQuality
SIO_000300: 5.887e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.98e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

GenotypeQuality
all individuals: 1425
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 395
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3700
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3580
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2468
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.017293997965412e-4
allele num: 9830
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25012
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3892
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

FS
type: SiteQuality
SIO_000300: 2.48e0

DP
type: SiteQuality
SIO_000300: 6.95306e5

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e0

VQSLOD
type: SiteQuality
SIO_000300: -2.599e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.21e-2

QD
type: SiteQuality
SIO_000300: 1.878e1

GenotypeQuality
all individuals: 583
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1263
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 654
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 402
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1460
bin: 9.75e1
variant carriers: 42

GenotypeQuality
all individuals: 252
bin: 8.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2450
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 7.905138339920949e-4
allele num: 2530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 7.720020586721565e-4
allele num: 3886
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2712
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 42
allele frequency: 1.68566383047038e-3
allele num: 24916
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

FS
type: SiteQuality
SIO_000300: 5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.13e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.263e1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

DP
type: SiteQuality
SIO_000300: 6.93237e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

GenotypeQuality
all individuals: 468
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3048
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 569
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 647
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variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 9.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.093327875562832e-5
allele num: 24430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2412
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

DP
type: SiteQuality
SIO_000300: 6.9094e5

VQSLOD
type: SiteQuality
SIO_000300: -2.836e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.175e1

FS
type: SiteQuality
SIO_000300: 1.2466e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.614e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.37e-2

GenotypeQuality
all individuals: 3137
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1419
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 569
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1582
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3854
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.02e-2

DP
type: SiteQuality
SIO_000300: 6.91889e5

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.35e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

QD
type: SiteQuality
SIO_000300: 7.45e0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
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variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3738
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
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variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25172
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.22e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.03644e5

VQSLOD
type: SiteQuality
SIO_000300: -1.808e0

MQ
type: SiteQuality
SIO_000300: 5.79e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.666e0

QD
type: SiteQuality
SIO_000300: 6.57e0

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

GenotypeQuality
all individuals: 1698
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3698
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24112
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25164
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9858
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.888024883359253e-4
allele num: 2572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

QD
type: SiteQuality
SIO_000300: 2.32e1

VQSLOD
type: SiteQuality
SIO_000300: -2.418e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-2

DP
type: SiteQuality
SIO_000300: 7.13266e5

GenotypeQuality
all individuals: 8512
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23966
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3802
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25246
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 1.262626262626263e-3
allele num: 3960
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 2.247e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.43e-1

FS
type: SiteQuality
SIO_000300: 1.947e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.07e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.889999999999999e-1

DP
type: SiteQuality
SIO_000300: 7.18777e5

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

GenotypeQuality
all individuals: 1162
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1651
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3745
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2488
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.009896990506968e-4
allele num: 9902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25246
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2660
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.846153846153846e-4
allele num: 2600
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.07e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 1.947e0

QD
type: SiteQuality
SIO_000300: 2.247e1

DP
type: SiteQuality
SIO_000300: 7.18777e5

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.889999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

GenotypeQuality
all individuals: 28073
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1802
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2916
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.443526170798898e-4
allele num: 2904
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27230
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.588e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

FS
type: SiteQuality
SIO_000300: 7.404e0

MQ
type: SiteQuality
SIO_000300: 5.805e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.63e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

QD
type: SiteQuality
SIO_000300: 7.84e0

VQSLOD
type: SiteQuality
SIO_000300: -1.582e0

DP
type: SiteQuality
SIO_000300: 7.41835e5

GenotypeQuality
all individuals: 1782
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 448
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 492
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2992
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.358490566037736e-3
allele num: 424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 3.25003611151235e-4
allele num: 27692
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.786651008025054e-5
allele num: 10218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2950
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4250
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

FS
type: SiteQuality
SIO_000300: 5.26e-1

QD
type: SiteQuality
SIO_000300: 1.546e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.51e-2

DP
type: SiteQuality
SIO_000300: 7.55783e5

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1331
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5392
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 179
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1879
bin: 3.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.502136303144918e-5
allele num: 28554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3138
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3060
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.293577981651376e-3
allele num: 436
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.739e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.66534e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.29e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

FS
type: SiteQuality
SIO_000300: 3.574e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.067e1

GenotypeQuality
all individuals: 364
bin: 5.75e1
variant carriers: 57

GenotypeQuality
all individuals: 345
bin: 8.75e1
variant carriers: 103

GenotypeQuality
all individuals: 5272
bin: 6.25e1
variant carriers: 86

GenotypeQuality
all individuals: 1863
bin: 3.75e1
variant carriers: 28

GenotypeQuality
all individuals: 1217
bin: 1.25e1
variant carriers: 15

GenotypeQuality
all individuals: 613
bin: 7.25e1
variant carriers: 71

GenotypeQuality
all individuals: 536
bin: 8.25e1
variant carriers: 100

Other
type: Population
allele count: 10
allele frequency: 2.232142857142857e-2
allele num: 448
num of homozygotes: 1

African
type: Population
allele count: 758
allele frequency: 1.540650406504065e-1
allele num: 4920
num of homozygotes: 43

South Asian
type: Population
allele count: 89
allele frequency: 8.493987402175988e-3
allele num: 10478
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 63
allele frequency: 2.232459248759745e-2
allele num: 2822
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3160
num of homozygotes: 0

Latino
type: Population
allele count: 173
allele frequency: 5.040792540792541e-2
allele num: 3432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2005
allele frequency: 6.575495211858848e-2
allele num: 30492
num of homozygotes: 48

QD
type: SiteQuality
SIO_000300: 1.374e1

FS
type: SiteQuality
SIO_000300: 2.522e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.153e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.91402e5

GenotypeQuality
all individuals: 491
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1059
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 9.455370650529501e-5
allele num: 10576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3290
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5066
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2924
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.351e0

DP
type: SiteQuality
SIO_000300: 8.11542e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

MQ
type: SiteQuality
SIO_000300: 5.876e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

QD
type: SiteQuality
SIO_000300: 1.732e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.02e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.19e-1

GenotypeQuality
all individuals: 617
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1526
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2442
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7211
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2988
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10714
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3830
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.949852507374631e-4
allele num: 3390
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 8.25494e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

QD
type: SiteQuality
SIO_000300: 7.1e0

GenotypeQuality
all individuals: 1555
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1527
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 508
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2477
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4181
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.024437454633438e-5
allele num: 33064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3422
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.279e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.197e0

DP
type: SiteQuality
SIO_000300: 8.30545e5

QD
type: SiteQuality
SIO_000300: 1.274e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.115e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.96e-1

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5436
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32248
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 3453
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2413
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 14
allele frequency: 8.518924181574784e-4
allele num: 16434
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.032631144155308e-4
allele num: 9684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66098
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

QD
type: SiteQuality
SIO_000300: 1.109e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 8.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.979e0

MQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

DP
type: SiteQuality
SIO_000300: 2.512458e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.69e-1

GenotypeQuality
all individuals: 344
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3994
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32268
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2432
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3515
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.431019812811474e-4
allele num: 16454
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.026176426085641e-5
allele num: 66090
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.739e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

DP
type: SiteQuality
SIO_000300: 2.51627e6

MQRankSum
type: SiteQuality
SIO_000300: -4.45e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

QD
type: SiteQuality
SIO_000300: 1.411e1

VQSLOD
type: SiteQuality
SIO_000300: 8.6e-1

GenotypeQuality
all individuals: 275
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32319
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2629
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3550
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6502
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9698
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.022152376922845e-5
allele num: 66178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.539e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

DP
type: SiteQuality
SIO_000300: 2.522838e6

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

QD
type: SiteQuality
SIO_000300: 1.421e1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

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

GenotypeQuality
all individuals: 257
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3583
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4091
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2638
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.214624073849144e-4
allele num: 16466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 2.524108e6

QD
type: SiteQuality
SIO_000300: 1.142e1

VQSLOD
type: SiteQuality
SIO_000300: 9.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.054e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3472
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32350
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4158
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66246
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.173e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.643e0

MQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e0

QD
type: SiteQuality
SIO_000300: 1.464e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

VQSLOD
type: SiteQuality
SIO_000300: 8.4e-1

DP
type: SiteQuality
SIO_000300: 2.530588e6

GenotypeQuality
all individuals: 32352
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4182
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7136
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.322880371660859e-4
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66254
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.62e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

VQSLOD
type: SiteQuality
SIO_000300: -5.114e-1

MQ
type: SiteQuality
SIO_000300: 5.871e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

DP
type: SiteQuality
SIO_000300: 2.533151e6

GenotypeQuality
all individuals: 2479
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3625
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7210
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
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: 66332
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -6.54e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.471e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.09e-1

FS
type: SiteQuality
SIO_000300: 7.033e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

DP
type: SiteQuality
SIO_000300: 2.536034e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.83e-1

QD
type: SiteQuality
SIO_000300: 1.08e1

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7262
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3625
bin: 8.25e1
variant carriers: 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: 1.507340749449821e-5
allele num: 66342
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
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: 894
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 1.11e-1

FS
type: SiteQuality
SIO_000300: 9.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

QD
type: SiteQuality
SIO_000300: 9.880000000000001e0

DP
type: SiteQuality
SIO_000300: 2.536554e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.484e0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32362
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3476
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4218
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3618
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66364
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: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

FS
type: SiteQuality
SIO_000300: 2.008e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 2.537663e6

VQSLOD
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

QD
type: SiteQuality
SIO_000300: 1.265e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

GenotypeQuality
all individuals: 32365
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 131
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3477
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506750241080039e-5
allele num: 66368
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-2

MQ
type: SiteQuality
SIO_000300: 5.943e1

FS
type: SiteQuality
SIO_000300: 1.246e0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 2.538024e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

QD
type: SiteQuality
SIO_000300: 1.107e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.66e-1

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2480
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3476
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66386
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.025430680885972e-4
allele num: 9752
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.21e0

VQSLOD
type: SiteQuality
SIO_000300: -1.012e0

QD
type: SiteQuality
SIO_000300: 8.49e0

MQRankSum
type: SiteQuality
SIO_000300: -3.37e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.856e0

DP
type: SiteQuality
SIO_000300: 2.538451e6

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3623
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3474
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3627
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2480
bin: 8.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -9.91e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: -2.389e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.53893e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.183e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.145e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.303e1