2-85626371-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626371
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626370
    reference: chr 2
allele count: 1
allele frequency: 8.344459279038718e-6
allele num: 119840
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.553delC
  hgvsp: ENSP00000403330.1:p.Leu185TrpfsTer36
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.553delC
  hgvsp: ENSP00000398232.2:p.Leu185TrpfsTer36
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.553delC
  hgvsp: ENSP00000386965.1:p.Leu185TrpfsTer36
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.553delC
  hgvsp: ENSP00000386596.1:p.Leu185TrpfsTer?
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.553delC
  hgvsp: ENSP00000387063.1:p.Leu185TrpfsTer31
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.553delC
  hgvsp: ENSP00000263867.4:p.Leu185TrpfsTer36
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.345delC
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.553delC
  hgvsp: ENSP00000386315.1:p.Leu185TrpfsTer36
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.553delC
  hgvsp: ENSP00000391923.1:p.Leu185TrpfsTer36
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.767delC
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7873
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu185TrpfsTer36
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: AG
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

2-85626385-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626385
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626385
    reference: chr 2
allele count: 1
allele frequency: 8.414391976035812e-6
allele num: 118844
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.540A>C
  hgvsp: ENST00000409921.1:c.540A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.540A>C
  hgvsp: ENST00000263867.4:c.540A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.540A>C
  hgvsp: ENST00000449030.1:c.540A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.540A>C
  hgvsp: ENST00000439385.1:c.540A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.540A>C
  hgvsp: ENST00000409275.1:c.540A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.332A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.540A>C
  hgvsp: ENST00000409670.1:c.540A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.540A>C
  hgvsp: ENST00000447219.2:c.540A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.754A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.540A>C
  hgvsp: ENST00000409724.1:c.540A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1841
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly180Gly
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

2-85626387-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626387
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626387
    reference: chr 2
allele count: 2
allele frequency: 1.688647224708286e-5
allele num: 118438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.538G>A
  hgvsp: ENSP00000386596.1:p.Gly180Arg
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.538G>A
  hgvsp: ENSP00000386315.1:p.Gly180Arg
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.538G>A
  hgvsp: ENSP00000391923.1:p.Gly180Arg
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.538G>A
  hgvsp: ENSP00000403330.1:p.Gly180Arg
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.330G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.538G>A
  hgvsp: ENSP00000398232.2:p.Gly180Arg
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.752G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.538G>A
  hgvsp: ENSP00000387063.1:p.Gly180Arg
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.538G>A
  hgvsp: ENSP00000386965.1:p.Gly180Arg
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.538G>A
  hgvsp: ENSP00000263867.4:p.Gly180Arg
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28437
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly180Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

2-85626400-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626400
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626400
    reference: chr 2
allele count: 27
allele frequency: 2.32730532521937e-4
allele num: 116014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.525C>T
  hgvsp: ENST00000449030.1:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.525C>T
  hgvsp: ENST00000439385.1:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.525C>T
  hgvsp: ENST00000409670.1:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.525C>T
  hgvsp: ENST00000409921.1:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.525C>T
  hgvsp: ENST00000409724.1:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.525C>T
  hgvsp: ENST00000263867.4:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.739C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.525C>T
  hgvsp: ENST00000447219.2:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.525C>T
  hgvsp: ENST00000409275.1:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.317C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6450
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 26119
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17679
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe175Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

2-85626424-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626424
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626424
    reference: chr 2
allele count: 2
allele frequency: 1.80772985285079e-5
allele num: 110636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.517-16T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.517-16T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.517-16T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.517-16T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.517-16T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.731-16T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.309-16T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.517-16T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.517-16T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.517-16T>C
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2186
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

2-85626426-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626426
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626426
    reference: chr 2
allele count: 1
allele frequency: 9.091570296021529e-6
allele num: 109992
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.517-18T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.517-18T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.731-18T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.517-18T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.517-18T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.517-18T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.309-18T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.517-18T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.517-18T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.517-18T>C
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15756
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1064
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

2-85626427-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626427
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626427
    reference: chr 2
allele count: 1
allele frequency: 9.099843482692098e-6
allele num: 109892
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.517-19C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.517-19C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.731-19C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.517-19C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.517-19C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.309-19C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.517-19C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.517-19C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.517-19C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.517-19C>G
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2818
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1436
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

2-85626430-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626430
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626430
    reference: chr 2
allele count: 6
allele frequency: 5.504385160177608e-5
allele num: 109004
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.517-22G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.731-22G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.517-22G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.517-22G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.309-22G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.517-22G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.517-22G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.517-22G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.517-22G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.517-22G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14149
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11096
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5967
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1438
  bin: 9.75e1
  variant carriers: 6
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-85626431-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626431
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626431
    reference: chr 2
allele count: 5
allele frequency: 4.591958562165935e-5
allele num: 108886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.517-23C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.731-23C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.517-23C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.309-23C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.517-23C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.517-23C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.517-23C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.517-23C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.517-23C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.517-23C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14088
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 13318
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22148
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

2-85626445-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626445
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626445
    reference: chr 2
allele count: 1
allele frequency: 9.414422895876483e-6
allele num: 106220
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.517-37A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.309-37A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.517-37A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.517-37A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.731-37A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.517-37A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.517-37A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.517-37A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.517-37A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.517-37A>C
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13937
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8592
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1423
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

2-85626447-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626447
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626447
    reference: chr 2
allele count: 1
allele frequency: 9.539618033693931e-6
allele num: 104826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.731-39G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.517-39G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.517-39G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.517-39G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.517-39G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.517-39G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.309-39G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.517-39G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.517-39G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.517-39G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19299
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9387
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

2-85626449-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626449
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626449
    reference: chr 2
allele count: 9
allele frequency: 8.646197594435692e-5
allele num: 104092
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.517-41A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.517-41A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.309-41A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.517-41A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.517-41A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.517-41A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.731-41A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.517-41A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.517-41A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.517-41A>G
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7181
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15763
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7453
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19136
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13111
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/2-85626454-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626454
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626454
    reference: chr 2
allele count: 5180
allele frequency: 5.045290737313723e-2
allele num: 102670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.517-46G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.517-46G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.517-46G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.517-46G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.731-46G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.517-46G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.517-46G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.517-46G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.309-46G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.517-46G>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15599
  bin: 1.75e1
  variant carriers: 1484
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 2.75e1
  variant carriers: 565
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 3.25e1
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8104
  bin: 2.25e1
  variant carriers: 1005
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 7.5e0
  variant carriers: 439
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 2.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 18933
  bin: 1.25e1
  variant carriers: 1375
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 149
genotype quality: GenotypeQuality
  all individuals: 5389
  bin: 2.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 7.25e1
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 11800
  bin: 2.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 6523
  bin: 3.75e1
  variant carriers: 38
num of homozygotes: 122
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

2-85626456-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626456
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626456
    reference: chr 2
allele count: 2
allele frequency: 1.968155248085969e-5
allele num: 101618
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.517-48A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.517-48A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.517-48A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.517-48A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.517-48A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.731-48A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.517-48A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.517-48A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.517-48A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.309-48A>G
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8393
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18988
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5889
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

2-85626459-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85626459
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85626458
    reference: chr 2
allele count: 3
allele frequency: 3.005108684764099e-5
allele num: 99830
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.517-52delG
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.517-52delG
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.517-52delG
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.731-52delG
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.517-52delG
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.517-52delG
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.517-52delG
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.517-52delG
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.309-52delG
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.517-52delG
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15330
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18791
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8876
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7333
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10864
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5770
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: TC
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

2-85628246-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628246
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628246
    reference: chr 2
allele count: 1
allele frequency: 8.412551526878102e-6
allele num: 118870
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.516+42T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.308+42T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.516+42T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.730+42T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.516+42T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.516+42T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.516+42T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.516+42T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.516+42T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.516+42T>C
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5648
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9349
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10233
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD

2-85628252-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628252
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628252
    reference: chr 2
allele count: 1
allele frequency: 8.416799932665601e-6
allele num: 118810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.516+36G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.516+36G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.516+36G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.516+36G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.308+36G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.516+36G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.516+36G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.730+36G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.516+36G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.516+36G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5646
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2755
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4049
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/2-85628258-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628258
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628258
    reference: chr 2
allele count: 77
allele frequency: 6.472002286213794e-4
allele num: 118974
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.730+30G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.516+30G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.516+30G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.516+30G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.516+30G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.516+30G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.516+30G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.516+30G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.308+30G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.516+30G>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7465
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 8685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10696
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4047
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

2-85628258-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628258
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628258
    reference: chr 2
allele count: 1
allele frequency: 8.405197774303629e-6
allele num: 118974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.516+30G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.516+30G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.516+30G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.516+30G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.730+30G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.308+30G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.516+30G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.516+30G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.516+30G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.516+30G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7465
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

2-85628259-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628259
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628259
    reference: chr 2
allele count: 1
allele frequency: 8.391092016715055e-6
allele num: 119174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.516+29C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.516+29C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.730+29C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.516+29C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.516+29C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.516+29C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.308+29C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.516+29C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.516+29C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.516+29C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

2-85628262-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628262
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628262
    reference: chr 2
allele count: 11
allele frequency: 9.218134584764938e-5
allele num: 119330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.516+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.516+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.516+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.308+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.516+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.516+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.516+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.516+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.730+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.516+26C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9609
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5420
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2338
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-85628280-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628280
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628280
    reference: chr 2
allele count: 1
allele frequency: 8.308684236764266e-6
allele num: 120356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.308+8G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.516+8G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.730+8G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.516+8G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.516+8G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.516+8G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.516+8G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.516+8G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.516+8G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.516+8G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
hgvs: c.516+8G>A
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

2-85628284-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628284
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628284
    reference: chr 2
allele count: 3
allele frequency: 2.488841693076042e-5
allele num: 120538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.516+4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.516+4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.516+4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.308+4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.516+4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.730+4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.516+4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.516+4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.516+4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.516+4G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10266
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3573
  bin: 9.25e1
  variant carriers: 0
hgvs: c.516+4G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

2-85628287-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628287
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628287
    reference: chr 2
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.516+1G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.516+1G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.308+1G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.516+1G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.516+1G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.516+1G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.516+1G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.730+1G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.516+1G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.516+1G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5609
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
hgvs: c.516+1G>A
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

2-85628294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628294
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628294
    reference: chr 2
allele count: 2
allele frequency: 1.654204989082247e-5
allele num: 120904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.510G>A
  hgvsp: ENST00000409921.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.302G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.510G>A
  hgvsp: ENST00000439385.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.510G>A
  hgvsp: ENST00000409670.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.510G>A
  hgvsp: ENST00000449030.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.510G>A
  hgvsp: ENST00000447219.2:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.510G>A
  hgvsp: ENST00000409275.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.724G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.510G>A
  hgvsp: ENST00000263867.4:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.510G>A
  hgvsp: ENST00000409724.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu170Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

2-85628296-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628296
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628296
    reference: chr 2
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.508C>G
  hgvsp: ENSP00000386315.1:p.Leu170Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.508C>G
  hgvsp: ENSP00000386965.1:p.Leu170Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.508C>G
  hgvsp: ENSP00000263867.4:p.Leu170Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.508C>G
  hgvsp: ENSP00000387063.1:p.Leu170Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.530C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.300C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.508C>G
  hgvsp: ENSP00000391923.1:p.Leu170Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.508C>G
  hgvsp: ENSP00000386596.1:p.Leu170Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.508C>G
  hgvsp: ENSP00000398232.2:p.Leu170Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.722C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.508C>G
  hgvsp: ENSP00000403330.1:p.Leu170Val
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3895
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu170Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

2-85628297-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628297
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628297
    reference: chr 2
allele count: 1
allele frequency: 8.263916435277007e-6
allele num: 121008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.507C>T
  hgvsp: ENST00000439385.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.507C>T
  hgvsp: ENST00000409724.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.529C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.721C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.299C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.507C>T
  hgvsp: ENST00000409670.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.507C>T
  hgvsp: ENST00000449030.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.507C>T
  hgvsp: ENST00000263867.4:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.507C>T
  hgvsp: ENST00000409275.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.507C>T
  hgvsp: ENST00000447219.2:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.507C>T
  hgvsp: ENST00000409921.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3895
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp169Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

2-85628305-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628305
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628305
    reference: chr 2
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.499A>G
  hgvsp: ENSP00000386965.1:p.Ile167Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.499A>G
  hgvsp: ENSP00000403330.1:p.Ile167Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.713A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.499A>G
  hgvsp: ENSP00000398232.2:p.Ile167Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.499A>G
  hgvsp: ENSP00000263867.4:p.Ile167Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.291A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.521A>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.499A>G
  hgvsp: ENSP00000387063.1:p.Ile167Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.499A>G
  hgvsp: ENSP00000391923.1:p.Ile167Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.499A>G
  hgvsp: ENSP00000386596.1:p.Ile167Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.499A>G
  hgvsp: ENSP00000386315.1:p.Ile167Val
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile167Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD

2-85628310-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628310
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628310
    reference: chr 2
allele count: 17
allele frequency: 1.402038729258074e-4
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.494G>A
  hgvsp: ENSP00000387063.1:p.Cys165Tyr
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.516G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.494G>A
  hgvsp: ENSP00000386965.1:p.Cys165Tyr
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.494G>A
  hgvsp: ENSP00000403330.1:p.Cys165Tyr
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.708G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.494G>A
  hgvsp: ENSP00000386315.1:p.Cys165Tyr
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.494G>A
  hgvsp: ENSP00000391923.1:p.Cys165Tyr
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.494G>A
  hgvsp: ENSP00000386596.1:p.Cys165Tyr
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.494G>A
  hgvsp: ENSP00000263867.4:p.Cys165Tyr
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.494G>A
  hgvsp: ENSP00000398232.2:p.Cys165Tyr
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.286G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys165Tyr
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/2-85628311-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628311
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628311
    reference: chr 2
allele count: 4
allele frequency: 3.298533801725133e-5
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.493T>G
  hgvsp: ENSP00000263867.4:p.Cys165Gly
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.285T>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.493T>G
  hgvsp: ENSP00000391923.1:p.Cys165Gly
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.493T>G
  hgvsp: ENSP00000386596.1:p.Cys165Gly
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.493T>G
  hgvsp: ENSP00000398232.2:p.Cys165Gly
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.493T>G
  hgvsp: ENSP00000386965.1:p.Cys165Gly
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.493T>G
  hgvsp: ENSP00000387063.1:p.Cys165Gly
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.493T>G
  hgvsp: ENSP00000386315.1:p.Cys165Gly
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.707T>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.515T>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.493T>G
  hgvsp: ENSP00000403330.1:p.Cys165Gly
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10802
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys165Gly
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-85628314-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628314
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628314
    reference: chr 2
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.490G>A
  hgvsp: ENSP00000386965.1:p.Asp164Asn
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.490G>A
  hgvsp: ENSP00000263867.4:p.Asp164Asn
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.490G>A
  hgvsp: ENSP00000403330.1:p.Asp164Asn
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.282G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.490G>A
  hgvsp: ENSP00000391923.1:p.Asp164Asn
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.490G>A
  hgvsp: ENSP00000386596.1:p.Asp164Asn
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.704G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.490G>A
  hgvsp: ENSP00000386315.1:p.Asp164Asn
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.490G>A
  hgvsp: ENSP00000398232.2:p.Asp164Asn
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.512G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.490G>A
  hgvsp: ENSP00000387063.1:p.Asp164Asn
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp164Asn
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

2-85628340-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628340
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628340
    reference: chr 2
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.464T>A
  hgvsp: ENSP00000263867.4:p.Leu155Gln
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.464T>A
  hgvsp: ENSP00000398232.2:p.Leu155Gln
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.464T>A
  hgvsp: ENSP00000403330.1:p.Leu155Gln
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.464T>A
  hgvsp: ENSP00000386965.1:p.Leu155Gln
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.464T>A
  hgvsp: ENSP00000387063.1:p.Leu155Gln
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.464T>A
  hgvsp: ENSP00000386315.1:p.Leu155Gln
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.464T>A
  hgvsp: ENSP00000386596.1:p.Leu155Gln
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.678T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.256T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.464T>A
  hgvsp: ENSP00000391923.1:p.Leu155Gln
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.486T>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu155Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

2-85628347-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628347
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628347
    reference: chr 2
allele count: 5
allele frequency: 4.118955432902216e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.457C>T
  hgvsp: ENSP00000386965.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.457C>T
  hgvsp: ENSP00000386315.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.457C>T
  hgvsp: ENSP00000391923.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.671C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.479C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.457C>T
  hgvsp: ENSP00000398232.2:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.249C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.457C>T
  hgvsp: ENSP00000263867.4:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.457C>T
  hgvsp: ENSP00000387063.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.457C>T
  hgvsp: ENSP00000403330.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.457C>T
  hgvsp: ENSP00000386596.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg153Trp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

2-85628349-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628349
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628349
    reference: chr 2
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.455A>T
  hgvsp: ENSP00000386315.1:p.Glu152Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.455A>T
  hgvsp: ENSP00000386596.1:p.Glu152Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.455A>T
  hgvsp: ENSP00000398232.2:p.Glu152Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.455A>T
  hgvsp: ENSP00000263867.4:p.Glu152Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.455A>T
  hgvsp: ENSP00000386965.1:p.Glu152Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.669A>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.455A>T
  hgvsp: ENSP00000391923.1:p.Glu152Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.247A>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.455A>T
  hgvsp: ENSP00000403330.1:p.Glu152Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.455A>T
  hgvsp: ENSP00000387063.1:p.Glu152Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.477A>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu152Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/2-85628350-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628350
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628350
    reference: chr 2
allele count: 4
allele frequency: 3.295001482750667e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.454G>T
  hgvsp: ENSP00000386315.1:p.Glu152Ter
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.454G>T
  hgvsp: ENSP00000403330.1:p.Glu152Ter
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.454G>T
  hgvsp: ENSP00000386965.1:p.Glu152Ter
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.668G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.454G>T
  hgvsp: ENSP00000398232.2:p.Glu152Ter
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.454G>T
  hgvsp: ENSP00000391923.1:p.Glu152Ter
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.246G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.454G>T
  hgvsp: ENSP00000263867.4:p.Glu152Ter
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.454G>T
  hgvsp: ENSP00000387063.1:p.Glu152Ter
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.454G>T
  hgvsp: ENSP00000386596.1:p.Glu152Ter
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.476G>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu152Ter
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

2-85628351-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628351
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628351
    reference: chr 2
allele count: 6
allele frequency: 4.942502224126001e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.453C>T
  hgvsp: ENST00000409921.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.453C>T
  hgvsp: ENST00000409275.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.453C>T
  hgvsp: ENST00000449030.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.245C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.453C>T
  hgvsp: ENST00000409724.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.453C>T
  hgvsp: ENST00000263867.4:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.453C>T
  hgvsp: ENST00000439385.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.453C>T
  hgvsp: ENST00000447219.2:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.667C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.453C>T
  hgvsp: ENST00000409670.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.475C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Thr151Thr
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

2-85628355-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628355
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628355
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.241C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.449C>T
  hgvsp: ENSP00000386315.1:p.Ala150Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.449C>T
  hgvsp: ENSP00000403330.1:p.Ala150Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.449C>T
  hgvsp: ENSP00000391923.1:p.Ala150Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.449C>T
  hgvsp: ENSP00000386965.1:p.Ala150Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.449C>T
  hgvsp: ENSP00000386596.1:p.Ala150Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.663C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.449C>T
  hgvsp: ENSP00000398232.2:p.Ala150Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.449C>T
  hgvsp: ENSP00000263867.4:p.Ala150Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.449C>T
  hgvsp: ENSP00000387063.1:p.Ala150Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.471C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala150Val
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

2-85628358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628358
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628358
    reference: chr 2
allele count: 4
allele frequency: 3.295055768818887e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.238G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.446G>A
  hgvsp: ENSP00000386596.1:p.Arg149His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.446G>A
  hgvsp: ENSP00000398232.2:p.Arg149His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.446G>A
  hgvsp: ENSP00000391923.1:p.Arg149His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.446G>A
  hgvsp: ENSP00000387063.1:p.Arg149His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.446G>A
  hgvsp: ENSP00000263867.4:p.Arg149His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.660G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.446G>A
  hgvsp: ENSP00000386965.1:p.Arg149His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.446G>A
  hgvsp: ENSP00000403330.1:p.Arg149His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.468G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.446G>A
  hgvsp: ENSP00000386315.1:p.Arg149His
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10902
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg149His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

2-85628359-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628359
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628359
    reference: chr 2
allele count: 5
allele frequency: 4.118819711023609e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.237C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.445C>T
  hgvsp: ENSP00000386596.1:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.445C>T
  hgvsp: ENSP00000386965.1:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.445C>T
  hgvsp: ENSP00000386315.1:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.467C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.445C>T
  hgvsp: ENSP00000403330.1:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.659C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.445C>T
  hgvsp: ENSP00000387063.1:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.445C>T
  hgvsp: ENSP00000263867.4:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.445C>T
  hgvsp: ENSP00000391923.1:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.445C>T
  hgvsp: ENSP00000398232.2:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg149Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

2-85628378-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628378
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628378
    reference: chr 2
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.426G>A
  hgvsp: ENST00000409670.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.426G>A
  hgvsp: ENST00000263867.4:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.640G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.218G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.426G>A
  hgvsp: ENST00000449030.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.426G>A
  hgvsp: ENST00000409275.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.448G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.426G>A
  hgvsp: ENST00000409724.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.426G>A
  hgvsp: ENST00000439385.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.426G>A
  hgvsp: ENST00000409921.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.426G>A
  hgvsp: ENST00000447219.2:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val142Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

2-85628385-TAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628385
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628383
    reference: chr 2
allele count: 5
allele frequency: 4.119226903494752e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.417_418delCT
  hgvsp: ENSP00000386596.1:p.Tyr140ProfsTer61
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.417_418delCT
  hgvsp: ENSP00000387063.1:p.Tyr140ProfsTer61
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.417_418delCT
  hgvsp: ENSP00000263867.4:p.Tyr140ProfsTer61
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.417_418delCT
  hgvsp: ENSP00000386965.1:p.Tyr140ProfsTer61
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.417_418delCT
  hgvsp: ENSP00000403330.1:p.Tyr140ProfsTer61
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.209_210delCT
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.417_418delCT
  hgvsp: ENSP00000391923.1:p.Tyr140ProfsTer61
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.417_418delCT
  hgvsp: ENSP00000398232.2:p.Tyr140ProfsTer61
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.631_632delCT
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.439_440delCT
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.417_418delCT
  hgvsp: ENSP00000386315.1:p.Tyr140ProfsTer61
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10921
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr140ProfsTer61
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: TAG
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

2-85628388-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628388
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628388
    reference: chr 2
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.208T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.416T>C
  hgvsp: ENSP00000386965.1:p.Leu139Pro
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.416T>C
  hgvsp: ENSP00000403330.1:p.Leu139Pro
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.416T>C
  hgvsp: ENSP00000263867.4:p.Leu139Pro
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.416T>C
  hgvsp: ENSP00000398232.2:p.Leu139Pro
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.416T>C
  hgvsp: ENSP00000386315.1:p.Leu139Pro
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.630T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.416T>C
  hgvsp: ENSP00000391923.1:p.Leu139Pro
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.416T>C
  hgvsp: ENSP00000386596.1:p.Leu139Pro
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.438T>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.416T>C
  hgvsp: ENSP00000387063.1:p.Leu139Pro
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu139Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

2-85628388-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628388
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628388
    reference: chr 2
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.416T>A
  hgvsp: ENSP00000391923.1:p.Leu139His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.208T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.416T>A
  hgvsp: ENSP00000386596.1:p.Leu139His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.416T>A
  hgvsp: ENSP00000386965.1:p.Leu139His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.416T>A
  hgvsp: ENSP00000403330.1:p.Leu139His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.416T>A
  hgvsp: ENSP00000387063.1:p.Leu139His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.630T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.416T>A
  hgvsp: ENSP00000263867.4:p.Leu139His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.416T>A
  hgvsp: ENSP00000386315.1:p.Leu139His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.416T>A
  hgvsp: ENSP00000398232.2:p.Leu139His
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.438T>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10920
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu139His
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

2-85628389-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628389
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628389
    reference: chr 2
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.415C>T
  hgvsp: ENSP00000391923.1:p.Leu139Phe
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.415C>T
  hgvsp: ENSP00000386596.1:p.Leu139Phe
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.415C>T
  hgvsp: ENSP00000387063.1:p.Leu139Phe
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.437C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.415C>T
  hgvsp: ENSP00000263867.4:p.Leu139Phe
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.415C>T
  hgvsp: ENSP00000386315.1:p.Leu139Phe
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.415C>T
  hgvsp: ENSP00000386965.1:p.Leu139Phe
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.207C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.415C>T
  hgvsp: ENSP00000398232.2:p.Leu139Phe
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.415C>T
  hgvsp: ENSP00000403330.1:p.Leu139Phe
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.629C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu139Phe
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

2-85628396-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628396
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628396
    reference: chr 2
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.408C>G
  hgvsp: ENSP00000263867.4:p.Ile136Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.408C>G
  hgvsp: ENSP00000403330.1:p.Ile136Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.408C>G
  hgvsp: ENSP00000386596.1:p.Ile136Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.408C>G
  hgvsp: ENSP00000398232.2:p.Ile136Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.408C>G
  hgvsp: ENSP00000386965.1:p.Ile136Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.622C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.408C>G
  hgvsp: ENSP00000386315.1:p.Ile136Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.200C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.408C>G
  hgvsp: ENSP00000391923.1:p.Ile136Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.430C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.408C>G
  hgvsp: ENSP00000387063.1:p.Ile136Met
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10922
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile136Met
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-85628426-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628426
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628426
    reference: chr 2
allele count: 4
allele frequency: 3.302237265747544e-5
allele num: 121130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.378C>T
  hgvsp: ENST00000447219.2:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.378C>T
  hgvsp: ENST00000439385.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.170C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.378C>T
  hgvsp: ENST00000409670.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.592C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.378C>T
  hgvsp: ENST00000409724.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.378C>T
  hgvsp: ENST00000449030.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.378C>T
  hgvsp: ENST00000263867.4:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.378C>T
  hgvsp: ENST00000409275.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.400C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.378C>T
  hgvsp: ENST00000409921.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10764
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8713
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His126His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ

2-85628433-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628433
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628433
    reference: chr 2
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.371C>T
  hgvsp: ENSP00000391923.1:p.Ala124Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.371C>T
  hgvsp: ENSP00000403330.1:p.Ala124Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.371C>T
  hgvsp: ENSP00000386965.1:p.Ala124Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.371C>T
  hgvsp: ENSP00000263867.4:p.Ala124Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.371C>T
  hgvsp: ENSP00000387063.1:p.Ala124Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.371C>T
  hgvsp: ENSP00000386596.1:p.Ala124Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.585C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.163C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.393C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.371C>T
  hgvsp: ENSP00000398232.2:p.Ala124Val
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.371C>T
  hgvsp: ENSP00000386315.1:p.Ala124Val
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala124Val
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

2-85628443-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628443
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628443
    reference: chr 2
allele count: 5
allele frequency: 4.144150117693863e-5
allele num: 120652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.361G>A
  hgvsp: ENSP00000398232.2:p.Val121Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.361G>A
  hgvsp: ENSP00000386965.1:p.Val121Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.361G>A
  hgvsp: ENSP00000387063.1:p.Val121Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.361G>A
  hgvsp: ENSP00000391923.1:p.Val121Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.383G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.361G>A
  hgvsp: ENSP00000403330.1:p.Val121Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.361G>A
  hgvsp: ENSP00000386596.1:p.Val121Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.361G>A
  hgvsp: ENSP00000263867.4:p.Val121Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.361G>A
  hgvsp: ENSP00000386315.1:p.Val121Met
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.575G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.153G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8709
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10488
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val121Met
num of homozygotes: 1
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

2-85628445-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628445
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628445
    reference: chr 2
allele count: 1
allele frequency: 8.292974192264313e-6
allele num: 120584
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.359G>A
  hgvsp: ENSP00000386315.1:p.Gly120Asp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.359G>A
  hgvsp: ENSP00000391923.1:p.Gly120Asp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.359G>A
  hgvsp: ENSP00000263867.4:p.Gly120Asp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.359G>A
  hgvsp: ENSP00000398232.2:p.Gly120Asp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.359G>A
  hgvsp: ENSP00000386965.1:p.Gly120Asp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.573G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.359G>A
  hgvsp: ENSP00000387063.1:p.Gly120Asp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.359G>A
  hgvsp: ENSP00000403330.1:p.Gly120Asp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.359G>A
  hgvsp: ENSP00000386596.1:p.Gly120Asp
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.151G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.381G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7470
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly120Asp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

2-85628456-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628456
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628456
    reference: chr 2
allele count: 5
allele frequency: 4.162920038631898e-5
allele num: 120108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.144-4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.352-4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.352-4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.352-4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.352-4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.352-4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.374-4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.352-4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.352-4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.566-4G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.352-4G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7469
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.352-4G>A
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

2-85628458-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628458
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628458
    reference: chr 2
allele count: 7
allele frequency: 5.833333333333333e-5
allele num: 120000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.566-6C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.374-6C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.352-6C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.352-6C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.144-6C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.352-6C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.352-6C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.352-6C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.352-6C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.352-6C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.352-6C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.352-6C>T
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/2-85628465-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628465
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628465
    reference: chr 2
allele count: 1
allele frequency: 8.351986102295126e-6
allele num: 119732
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.352-13G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.352-13G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.352-13G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.352-13G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.352-13G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.374-13G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.144-13G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.566-13G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.352-13G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.352-13G>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.352-13G>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

2-85628465-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628465
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628465
    reference: chr 2
allele count: 8
allele frequency: 6.681588881836101e-5
allele num: 119732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.352-13G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.374-13G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.352-13G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.352-13G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.352-13G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.352-13G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.566-13G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.352-13G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.352-13G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.144-13G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.352-13G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7462
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8655
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

2-85628466-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628466
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628466
    reference: chr 2
allele count: 4
allele frequency: 3.341017673983495e-5
allele num: 119724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.352-14C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.352-14C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.144-14C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.566-14C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.352-14C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.352-14C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.352-14C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.352-14C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.352-14C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.374-14C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.352-14C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10473
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9568
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

2-85628477-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628477
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628477
    reference: chr 2
allele count: 3
allele frequency: 2.514921869760579e-5
allele num: 119288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.144-25C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.352-25C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.352-25C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.352-25C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.352-25C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.374-25C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.566-25C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.352-25C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.352-25C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.352-25C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.352-25C>G
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8560
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7430
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP

2-85628478-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628478
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628477
    reference: chr 2
allele count: 2
allele frequency: 1.677261367638919e-5
allele num: 119242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.374-27delC
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.352-27delC
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.352-27delC
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.352-27delC
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.352-27delC
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.352-27delC
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.144-27delC
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.352-27delC
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.566-27delC
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.352-27delC
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.352-27delC
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: TG
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

2-85628483-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628483
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628483
    reference: chr 2
allele count: 2
allele frequency: 1.680135754969001e-5
allele num: 119038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.352-31A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.352-31A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.374-31A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.566-31A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.352-31A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.144-31A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.352-31A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.352-31A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.352-31A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.352-31A>C
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.352-31A>C
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8501
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7418
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4119
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

2-85628491-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628491
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628491
    reference: chr 2
allele count: 1
allele frequency: 8.43340979624882e-6
allele num: 118576
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.352-39C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.352-39C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.374-39C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.352-39C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.352-39C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.352-39C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.144-39C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.352-39C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.566-39C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.352-39C>G
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.352-39C>G
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

2-85628502-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628502
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628502
    reference: chr 2
allele count: 2
allele frequency: 1.698311877993275e-5
allele num: 117764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.352-50G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.352-50G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.566-50G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.352-50G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.352-50G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.352-50G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.352-50G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.374-50G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.144-50G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.352-50G>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.352-50G>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8283
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

2-85628613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628613
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628613
    reference: chr 2
allele count: 1
allele frequency: 8.265555775970376e-6
allele num: 120984
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.565+39C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.351+39C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.351+39C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.351+39C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.351+39C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.373+39C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.351+39C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.143+39C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.351+39C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.351+39C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.351+39C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

2-85628615-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628615
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628615
    reference: chr 2
allele count: 6
allele frequency: 4.959087527894868e-5
allele num: 120990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.351+37T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.351+37T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.373+37T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.351+37T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.565+37T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.351+37T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.351+37T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.143+37T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.351+37T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.351+37T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.351+37T>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11991
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum

2-85628624-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628624
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628624
    reference: chr 2
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.351+28C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.351+28C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.143+28C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.373+28C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.565+28C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.351+28C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.351+28C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.351+28C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.351+28C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.351+28C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.351+28C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12047
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16896
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-85628626-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628626
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628626
    reference: chr 2
allele count: 1
allele frequency: 8.260093834665961e-6
allele num: 121064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.373+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.351+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.351+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.351+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.565+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.351+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.351+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.351+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.143+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.351+26C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.351+26C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12070
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

2-85628626-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628626
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628626
    reference: chr 2
allele count: 6
allele frequency: 4.956056300799577e-5
allele num: 121064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.565+26C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.351+26C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.373+26C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.351+26C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.351+26C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.351+26C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.351+26C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.351+26C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.351+26C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.143+26C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.351+26C>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12639
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4945
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

2-85628630-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628630
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628630
    reference: chr 2
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.351+22C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.565+22C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.351+22C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.351+22C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.351+22C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.351+22C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.351+22C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.143+22C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.351+22C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.351+22C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.373+22C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12083
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

2-85628638-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628638
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628638
    reference: chr 2
allele count: 53
allele frequency: 4.374814276752402e-4
allele num: 121148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.351+14T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.143+14T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.373+14T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.351+14T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.351+14T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.565+14T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.351+14T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.351+14T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.351+14T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.351+14T>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.351+14T>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12112
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6645
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4525
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

2-85628639-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628639
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628639
    reference: chr 2
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.351+13C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.351+13C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.351+13C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.351+13C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.351+13C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.143+13C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.373+13C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.565+13C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.351+13C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.351+13C>A
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.351+13C>A
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

2-85628640-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85628640
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 85628640
    reference: chr 2
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000263867
  ensembl transcript: ENST00000263867
  gene symbol: CAPG
  hgvsc: ENST00000263867.4:c.351+12C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000459793
  gene symbol: CAPG
  hgvsc: ENST00000459793.2:n.565+12C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000403330
  ensembl transcript: ENST00000449030
  gene symbol: CAPG
  hgvsc: ENST00000449030.1:c.351+12C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000415012
  gene symbol: CAPG
  hgvsc: ENST00000415012.1:n.373+12C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386965
  ensembl transcript: ENST00000409724
  gene symbol: CAPG
  hgvsc: ENST00000409724.1:c.351+12C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl transcript: ENST00000483659
  gene symbol: CAPG
  hgvsc: ENST00000483659.1:n.143+12C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386315
  ensembl transcript: ENST00000409670
  gene symbol: CAPG
  hgvsc: ENST00000409670.1:c.351+12C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000387063
  ensembl transcript: ENST00000409921
  gene symbol: CAPG
  hgvsc: ENST00000409921.1:c.351+12C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000398232
  ensembl transcript: ENST00000447219
  gene symbol: CAPG
  hgvsc: ENST00000447219.2:c.351+12C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000386596
  ensembl transcript: ENST00000409275
  gene symbol: CAPG
  hgvsc: ENST00000409275.1:c.351+12C>T
  variant of: http://identifiers.org/hgnc/1474
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042493
  ensembl protein: ENSP00000391923
  ensembl transcript: ENST00000439385
  gene symbol: CAPG
  hgvsc: ENST00000439385.1:c.351+12C>T
  variant of: http://identifiers.org/hgnc/1474
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

GenotypeQuality
all individuals: 234
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7509
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 135
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516530178950561e-5
allele num: 65940
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

FS
type: SiteQuality
SIO_000300: 3.555e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

QD
type: SiteQuality
SIO_000300: 1.27e1

DP
type: SiteQuality
SIO_000300: 1.608569e6

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

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 296
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7196
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42363
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1860
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.583202e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.826e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 3.118e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.48e-1

QD
type: SiteQuality
SIO_000300: 1.776e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.16e-1

GenotypeQuality
all individuals: 1777
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7056
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2629
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41882
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 915
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.066073892380806e-5
allele num: 65230
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16092
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.79e-1

QD
type: SiteQuality
SIO_000300: 1.382e1

DP
type: SiteQuality
SIO_000300: 1.575504e6

FS
type: SiteQuality
SIO_000300: 5.583e0

VQSLOD
type: SiteQuality
SIO_000300: 8.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.565e0

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.85e-1

GenotypeQuality
all individuals: 39320
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4833
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1515
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6260
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 9.75e1
variant carriers: 27

GenotypeQuality
all individuals: 687
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 986
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1550
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.036688957166094e-5
allele num: 11066
num of homozygotes: 0

African
type: Population
allele count: 21
allele frequency: 2.14987714987715e-3
allele num: 9768
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.812744148254633e-5
allele num: 63998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15804
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.86e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.02e-1

QD
type: SiteQuality
SIO_000300: 1.276e1

MQ
type: SiteQuality
SIO_000300: 5.957e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.514878e6

GenotypeQuality
all individuals: 27457
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4166
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11958
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4259
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3463
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 561
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.317175974710221e-4
allele num: 15184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9218
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61252
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.233e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.295123e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
all individuals: 5318
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23458
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12682
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4040
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2827
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 596
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1085
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3687
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.641012176310348e-5
allele num: 60938
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10502
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.248991e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

FS
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.19e-1

QD
type: SiteQuality
SIO_000300: 1.224e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

GenotypeQuality
all individuals: 1075
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5310
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12701
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3655
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4035
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23784
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.642359742477992e-5
allele num: 60888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15078
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9142
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.248191e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

FS
type: SiteQuality
SIO_000300: 2.447e0

MQRankSum
type: SiteQuality
SIO_000300: -6.52e-1

QD
type: SiteQuality
SIO_000300: 1.163e1

GenotypeQuality
all individuals: 218
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4394
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3370
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13184
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21641
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.5e0
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GenotypeQuality
all individuals: 332
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 940
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3342
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7648
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.2531328320802e-3
allele num: 798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.653657891255457e-5
allele num: 60472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9032
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.670940170940171e-4
allele num: 14976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5672
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.091e1

FS
type: SiteQuality
SIO_000300: 8.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.149999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.214653e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.94e-1

GenotypeQuality
all individuals: 3322
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4398
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5938
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
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variant carriers: 0

GenotypeQuality
all individuals: 3291
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 4.25e1
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GenotypeQuality
all individuals: 1433
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14978
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5660
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.280064915708939e-5
allele num: 60386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9032
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.074e0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e-1

QD
type: SiteQuality
SIO_000300: 2.497e1

DP
type: SiteQuality
SIO_000300: 1.211217e6

GenotypeQuality
all individuals: 6264
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
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variant carriers: 0

GenotypeQuality
all individuals: 12414
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5625
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2087
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14650
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.798157946306095e-5
allele num: 10206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7420
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.03e0

DP
type: SiteQuality
SIO_000300: 1.083872e6

VQSLOD
type: SiteQuality
SIO_000300: -1.537e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.812e0

FS
type: SiteQuality
SIO_000300: 2.197e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

QD
type: SiteQuality
SIO_000300: 1.45e1

GenotypeQuality
all individuals: 809
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6910
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8957
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13308
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5722
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1423
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2588
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2179
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5358
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.906077348066299e-5
allele num: 14480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.03e-1

QD
type: SiteQuality
SIO_000300: 1.077e1

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-1

FS
type: SiteQuality
SIO_000300: 4.714e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

DP
type: SiteQuality
SIO_000300: 1.061971e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 3174
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2736
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5775
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8466
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9035
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
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GenotypeQuality
all individuals: 2068
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7060
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 9.75e1
variant carriers: 10

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.728548710502662e-5
allele num: 57852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 1.105888858169754e-3
allele num: 7234
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.366e0

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.747e0

QD
type: SiteQuality
SIO_000300: 1.023e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

DP
type: SiteQuality
SIO_000300: 1.052558e6

GenotypeQuality
all individuals: 1683
bin: 1.75e1
variant carriers: 16

GenotypeQuality
all individuals: 309
bin: 9.25e1
variant carriers: 54

GenotypeQuality
all individuals: 1104
bin: 7.5e0
variant carriers: 8

GenotypeQuality
all individuals: 6189
bin: 6.25e1
variant carriers: 54

GenotypeQuality
all individuals: 489
bin: 8.25e1
variant carriers: 83

GenotypeQuality
all individuals: 1111
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 257
bin: 8.75e1
variant carriers: 89

GenotypeQuality
all individuals: 2747
bin: 4.25e1
variant carriers: 35

GenotypeQuality
all individuals: 8398
bin: 3.25e1
variant carriers: 28

GenotypeQuality
all individuals: 486
bin: 2.5e0
variant carriers: 4

GenotypeQuality
all individuals: 264
bin: 5.75e1
variant carriers: 48

GenotypeQuality
all individuals: 3518
bin: 4.75e1
variant carriers: 33

GenotypeQuality
all individuals: 6021
bin: 9.75e1
variant carriers: 4776

GenotypeQuality
all individuals: 1763
bin: 6.75e1
variant carriers: 49

GenotypeQuality
all individuals: 717
bin: 7.75e1
variant carriers: 71

GenotypeQuality
all individuals: 1329
bin: 5.25e1
variant carriers: 41

Other
type: Population
allele count: 41
allele frequency: 5.437665782493369e-2
allele num: 754
num of homozygotes: 1

South Asian
type: Population
allele count: 852
allele frequency: 5.982305855919112e-2
allele num: 14242
num of homozygotes: 20

African
type: Population
allele count: 365
allele frequency: 4.330802088277171e-2
allele num: 8428
num of homozygotes: 9

Latino
type: Population
allele count: 291
allele frequency: 2.959121415497254e-2
allele num: 9834
num of homozygotes: 4

European (Finnish)
type: Population
allele count: 92
allele frequency: 1.755055322396032e-2
allele num: 5242
num of homozygotes: 0

East Asian
type: Population
allele count: 16
allele frequency: 2.248454187745925e-3
allele num: 7116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3523
allele frequency: 6.174851894696252e-2
allele num: 57054
num of homozygotes: 88

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.769e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

FS
type: SiteQuality
SIO_000300: 8.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

QD
type: SiteQuality
SIO_000300: 1.393e1

DP
type: SiteQuality
SIO_000300: 1.039222e6

GenotypeQuality
all individuals: 9335
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7296
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1856
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4416
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11946
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2587
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 2.5e0
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GenotypeQuality
all individuals: 2277
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GenotypeQuality
all individuals: 469
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3124
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5221
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 5.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.536818278276862e-5
allele num: 56548
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14060
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

DP
type: SiteQuality
SIO_000300: 1.023864e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 1.588e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

GenotypeQuality
all individuals: 708
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 7.5e0
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GenotypeQuality
all individuals: 3866
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9300
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3619
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4652
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 7.75e1
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GenotypeQuality
all individuals: 586
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variant carriers: 0

GenotypeQuality
all individuals: 3168
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.399956800345597e-5
allele num: 55556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5050
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6900
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13902
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

DP
type: SiteQuality
SIO_000300: 1.018301e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

QD
type: SiteQuality
SIO_000300: 1.241e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 1.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.418e0

FS
type: SiteQuality
SIO_000300: 1.711e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

GenotypeQuality
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variant carriers: 1

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14872
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65916
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 7.2e-3

MQ
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MQRankSum
type: SiteQuality
SIO_000300: -3.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.95e-1

DP
type: SiteQuality
SIO_000300: 2.324312e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 3.09e-1

QD
type: SiteQuality
SIO_000300: 1.516e1

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65898
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: 8652
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.74399784192069e-5
allele num: 14828
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.01e-1

FS
type: SiteQuality
SIO_000300: 2.015e0

DP
type: SiteQuality
SIO_000300: 2.327474e6

VQSLOD
type: SiteQuality
SIO_000300: 1.93e-1

QD
type: SiteQuality
SIO_000300: 1.572e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQRankSum
type: SiteQuality
SIO_000300: 4.38e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 77

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.676301351532182e-4
allele num: 14946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 71
allele frequency: 1.076638461771753e-3
allele num: 65946
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.499e0

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.392e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 2.335736e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 5.91e0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516392199678525e-5
allele num: 65946
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14946
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

QD
type: SiteQuality
SIO_000300: 1.392e1

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.499e0

VQSLOD
type: SiteQuality
SIO_000300: 5.91e0

DP
type: SiteQuality
SIO_000300: 2.335736e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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African
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Other
type: Population
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

East Asian
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African
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Other
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European (Non-Finnish)
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allele frequency: 1.665505859552433e-4
allele num: 66046
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European (Finnish)
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num of homozygotes: 0

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

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

Latino
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African
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South Asian
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European (Non-Finnish)
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allele num: 66512
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East Asian
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Other
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VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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DP
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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allele num: 8654
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Latino
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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South Asian
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Other
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ClippingRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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FS
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VQSLOD
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
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Other
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South Asian
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European (Finnish)
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East Asian
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Latino
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DP
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
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FS
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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Other
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European (Finnish)
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Latino
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African
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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MQ
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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European (Non-Finnish)
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East Asian
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African
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Other
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European (Finnish)
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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South Asian
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VQSLOD
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ClippingRankSum
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DP
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FS
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BaseQRankSum
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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ReadPosRankSum
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SIO_000300: 1.1e0

GenotypeDepth
all individuals: 1171
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 68
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4061
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23568
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14128
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3572
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2345
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5717
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2842
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.051e1

FS
type: SiteQuality
SIO_000300: 3.924e0

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.242e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
SIO_000300: 9.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

DP
type: SiteQuality
SIO_000300: 2.374823e6

GenotypeDepth
all individuals: 8717
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2840
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3572
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14236
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23
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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
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23565
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5734
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998141152485459e-5
allele num: 66708
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 8654
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.936e1

QD
type: SiteQuality
SIO_000300: 1.262e1

FS
type: SiteQuality
SIO_000300: 4.067e0

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.376307e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e-1

GenotypeDepth
all individuals: 8717
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4312
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3572
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23565
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2343
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2841
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.496537665997182e-5
allele num: 66718
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.94e1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

DP
type: SiteQuality
SIO_000300: 2.376762e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.05e-1

QD
type: SiteQuality
SIO_000300: 1.263e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

GenotypeDepth
all individuals: 389
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4312
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 2842
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 4064
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variant carriers: 0

GenotypeQuality
all individuals: 5735
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 3572
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23561
bin: 9.75e1
variant carriers: 1

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.903e0

VQSLOD
type: SiteQuality
SIO_000300: -1.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

DP
type: SiteQuality
SIO_000300: 2.37614e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 5.9e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.257e1

GenotypeDepth
all individuals: 10924
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variant carriers: 0

GenotypeQuality
all individuals: 2842
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23559
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variant carriers: 4

GenotypeQuality
all individuals: 5734
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3572
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4064
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4312
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994844433786943e-5
allele num: 66724
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.216e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.34e-1

DP
type: SiteQuality
SIO_000300: 2.376497e6

QD
type: SiteQuality
SIO_000300: 1.301e1

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4064
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5735
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 1

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.101e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 5.2e-1

QD
type: SiteQuality
SIO_000300: 1.734e1

VQSLOD
type: SiteQuality
SIO_000300: -2.926e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

DP
type: SiteQuality
SIO_000300: 2.3764e6

GenotypeDepth
all individuals: 277
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 3
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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
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4063
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
SIO_000300: -1.906e0

MQ
type: SiteQuality
SIO_000300: 5.82e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.953e0

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.61e-1

DP
type: SiteQuality
SIO_000300: 2.376039e6

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 5.995024129972123e-5
allele num: 66722
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
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SIO_000300: 1.314e1

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

FS
type: SiteQuality
SIO_000300: 1.792e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 2.376324e6

GenotypeDepth
all individuals: 352
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 5.995024129972123e-5
allele num: 66722
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 2.376294e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: 8.110000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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SIO_000300: 1.434e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQRankSum
type: SiteQuality
SIO_000300: -4.28e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2840
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.375869e6

BaseQRankSum
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SIO_000300: -4.478e0

MQRankSum
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SIO_000300: 1.67e0

MQ
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SIO_000300: 5.959e1

ReadPosRankSum
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SIO_000300: 3.1e-1

ClippingRankSum
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SIO_000300: 1.61e0

FS
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SIO_000300: 6.383e0

VQSLOD
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SIO_000300: -4.81e-2

InbreedingCoeff
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.151e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 5

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

GenotypeQuality
all individuals: 4062
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.995563283170454e-5
allele num: 66716
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-1

FS
type: SiteQuality
SIO_000300: 2.604e0

MQ
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SIO_000300: 5.985e1

DP
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SIO_000300: 2.375676e6

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.646e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.73e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 23544
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variant carriers: 1

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 9.615384615384615e-5
allele num: 10400
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East Asian
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Other
type: Population
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DP
type: SiteQuality
SIO_000300: 2.375799e6

InbreedingCoeff
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SIO_000300: 0.0e0

QD
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FS
type: SiteQuality
SIO_000300: 4.36e-1

MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.48e-1

GenotypeDepth
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variant carriers: 1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

European (Finnish)
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Other
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South Asian
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ReadPosRankSum
type: SiteQuality
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MQ
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DP
type: SiteQuality
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MQRankSum
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VQSLOD
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QD
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ClippingRankSum
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SIO_000300: 7.48e-1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 4.36e-1

InbreedingCoeff
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

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

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

African
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num of homozygotes: 0

Latino
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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

BaseQRankSum
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SIO_000300: 1.49e0

DP
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QD
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MQ
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InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: 3.45e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

Other
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South Asian
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allele frequency: 2.443792766373412e-4
allele num: 16368
num of homozygotes: 0

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

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

East Asian
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ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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QD
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66600
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Other
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num of homozygotes: 0

East Asian
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allele num: 8650
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South Asian
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BaseQRankSum
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SIO_000300: -3.754e0

MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQ
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FS
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QD
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ReadPosRankSum
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DP
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SIO_000300: 2.365621e6

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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allele frequency: 3.106747856343979e-4
allele num: 16094
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African
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MQRankSum
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DP
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InbreedingCoeff
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FS
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ReadPosRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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SIO_000300: -5.51e-1

VQSLOD
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
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African
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South Asian
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allele num: 16050
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

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

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

South Asian
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num of homozygotes: 0

Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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allele frequency: 5.789717461787865e-4
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Latino
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ReadPosRankSum
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MQ
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 2

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

South Asian
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East Asian
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allele frequency: 8.107482047718323e-4
allele num: 8634
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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Other
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

Other
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South Asian
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.363e1

FS
type: SiteQuality
SIO_000300: 1.596e0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 2.32442e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.515151515151515e-4
allele num: 6600
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15544
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.128668171557562e-3
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.067279211751194e-5
allele num: 66172
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
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SIO_000300: 1.363e1

BaseQRankSum
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SIO_000300: 3.44e0

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

FS
type: SiteQuality
SIO_000300: 1.596e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

DP
type: SiteQuality
SIO_000300: 2.32442e6

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511213201958532e-5
allele num: 66172
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.287166945552838e-4
allele num: 15538
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

QD
type: SiteQuality
SIO_000300: 1.338e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.19e-1

FS
type: SiteQuality
SIO_000300: 1.57e0

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e-1

DP
type: SiteQuality
SIO_000300: 2.322103e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 932
bin: 2.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.543114153314959e-5
allele num: 66034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15290
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

QD
type: SiteQuality
SIO_000300: 1.483e1

FS
type: SiteQuality
SIO_000300: 5.407e0

VQSLOD
type: SiteQuality
SIO_000300: 7.51e-1

DP
type: SiteQuality
SIO_000300: 2.301163e6

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 1150
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.309929263819754e-4
allele num: 15268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66014
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

DP
type: SiteQuality
SIO_000300: 2.298437e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.012e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.444e1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65932
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.322880371660859e-4
allele num: 8610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15168
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.474e1

MQ
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: 2.53e-1

DP
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SIO_000300: 2.285181e6

ReadPosRankSum
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SIO_000300: -3.62e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

BaseQRankSum
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SIO_000300: 3.65e-1

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

South Asian
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allele count: 1
allele frequency: 6.694336591243807e-5
allele num: 14938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65756
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.905e0

InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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BaseQRankSum
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MQRankSum
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QD
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MQ
type: SiteQuality
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DP
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SIO_000300: 2.262103e6

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

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

African
type: Population
allele count: 0
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: 14598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.055114261273371e-5
allele num: 65464
num of homozygotes: 0

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

Other
type: Population
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allele num: 858
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MQRankSum
type: SiteQuality
SIO_000300: -1.86e-1

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.502990951994469e-5
allele num: 66534
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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ClippingRankSum
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BaseQRankSum
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QD
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MQRankSum
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MQ
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VQSLOD
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SIO_000300: 1.6e0

DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 6.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.89e-1

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
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allele frequency: 5.182242183451373e-4
allele num: 11578
num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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VQSLOD
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DP
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FS
type: SiteQuality
SIO_000300: 5.669999999999999e-1

ClippingRankSum
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SIO_000300: -1.35e-1

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele num: 16354
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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QD
type: SiteQuality
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VQSLOD
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FS
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DP
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: -3.097e0

ReadPosRankSum
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SIO_000300: 6.44e-1

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

South Asian
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allele count: 1
allele frequency: 6.11545988258317e-5
allele num: 16352
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.659999999999999e-1

InbreedingCoeff
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SIO_000300: 3.0e-4

MQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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SIO_000300: 1.04e0

MQ
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SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.285e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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African
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South Asian
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allele num: 16352
num of homozygotes: 0

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

South Asian
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allele num: 16370
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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Latino
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European (Finnish)
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African
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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BaseQRankSum
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ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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African
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allele frequency: 4.902903287829264e-3
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Latino
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East Asian
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Other
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QD
type: SiteQuality
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

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

Latino
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66602
num of homozygotes: 0

DP
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
type: SiteQuality
SIO_000300: 9.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.76e-1

QD
type: SiteQuality
SIO_000300: 1.104e1

VQSLOD
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 1.399e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

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

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3992
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16108
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4399
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16862
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8011
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2567
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3089
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501501501501501e-5
allele num: 66600
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.432e0