1-150199063-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199063
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199063
    reference: chr 1
allele count: 2
allele frequency: 1.649675014022238e-5
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.435A>G
  hgvsp: ENST00000436748.2:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.558A>G
  hgvsp: ENST00000314136.8:c.558A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.162A>G
  hgvsp: ENST00000369115.2:c.162A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.392A>G
  hgvsp: ENSP00000435215.1:p.Lys131Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.162A>G
  hgvsp: ENST00000369116.4:c.162A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.192A>G
  hgvsp: ENST00000534220.1:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.414A>G
  hgvsp: ENST00000369119.3:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3497A>G
  variant of: http://identifiers.org/hgnc/16673
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17479
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys131Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

1-150199074-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199074
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199074
    reference: chr 1
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.151G>A
  hgvsp: ENSP00000358111.2:p.Gly51Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.151G>A
  hgvsp: ENSP00000358112.4:p.Gly51Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.403G>A
  hgvsp: ENSP00000358115.3:p.Gly135Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.547G>A
  hgvsp: ENSP00000324074.8:p.Gly183Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.181G>A
  hgvsp: ENSP00000436529.1:p.Gly61Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.381G>A
  hgvsp: ENST00000533654.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.424G>A
  hgvsp: ENSP00000393718.2:p.Gly142Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3508G>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3382
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3843
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly183Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

1-150199077-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199077
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199077
    reference: chr 1
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.421G>A
  hgvsp: ENSP00000393718.2:p.Glu141Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.378G>A
  hgvsp: ENST00000533654.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.400G>A
  hgvsp: ENSP00000358115.3:p.Glu134Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.544G>A
  hgvsp: ENSP00000324074.8:p.Glu182Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.178G>A
  hgvsp: ENSP00000436529.1:p.Glu60Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.148G>A
  hgvsp: ENSP00000358111.2:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.148G>A
  hgvsp: ENSP00000358112.4:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3511G>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3826
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17795
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7563
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu182Lys
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum

1-150199078-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199078
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199078
    reference: chr 1
allele count: 2
allele frequency: 1.649402916144356e-5
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.377G>A
  hgvsp: ENSP00000435215.1:p.Arg126Gln
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.543G>A
  hgvsp: ENST00000314136.8:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.420G>A
  hgvsp: ENST00000436748.2:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.177G>A
  hgvsp: ENST00000534220.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.147G>A
  hgvsp: ENST00000369115.2:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.147G>A
  hgvsp: ENST00000369116.4:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.399G>A
  hgvsp: ENST00000369119.3:c.399G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3512G>A
  variant of: http://identifiers.org/hgnc/16673
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4722
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1962
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg126Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

1-150199079-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199079
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199079
    reference: chr 1
allele count: 9
allele frequency: 7.427948895711598e-5
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.146C>T
  hgvsp: ENSP00000358112.4:p.Pro49Leu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.146C>T
  hgvsp: ENSP00000358111.2:p.Pro49Leu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.419C>T
  hgvsp: ENSP00000393718.2:p.Pro140Leu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.542C>T
  hgvsp: ENSP00000324074.8:p.Pro181Leu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3513C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.376C>T
  hgvsp: ENSP00000435215.1:p.Arg126Trp
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.176C>T
  hgvsp: ENSP00000436529.1:p.Pro59Leu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.398C>T
  hgvsp: ENSP00000358115.3:p.Pro133Leu
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7767
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14990
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3325
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17768
  bin: 9.75e1
  variant carriers: 9
hgvs: p.Pro181Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

1-150199097-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199097
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199097
    reference: chr 1
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.401A>T
  hgvsp: ENSP00000393718.2:p.Glu134Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.128A>T
  hgvsp: ENSP00000358112.4:p.Glu43Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.158A>T
  hgvsp: ENSP00000436529.1:p.Glu53Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.358A>T
  hgvsp: ENSP00000435215.1:p.Lys120Ter
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.380A>T
  hgvsp: ENSP00000358115.3:p.Glu127Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.128A>T
  hgvsp: ENSP00000358111.2:p.Glu43Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3531A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.524A>T
  hgvsp: ENSP00000324074.8:p.Glu175Val
  variant of: http://identifiers.org/hgnc/16673
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16831
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3743
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4590
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys120Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD

1-150199100-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199100
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199100
    reference: chr 1
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.125A>G
  hgvsp: ENSP00000358111.2:p.Glu42Gly
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.155A>G
  hgvsp: ENSP00000436529.1:p.Glu52Gly
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.521A>G
  hgvsp: ENSP00000324074.8:p.Glu174Gly
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.377A>G
  hgvsp: ENSP00000358115.3:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.355A>G
  hgvsp: ENSP00000435215.1:p.Arg119Gly
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.125A>G
  hgvsp: ENSP00000358112.4:p.Glu42Gly
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.398A>G
  hgvsp: ENSP00000393718.2:p.Glu133Gly
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3534A>G
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14638
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17223
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17728
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3235
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2900
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu174Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

1-150199104-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199104
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199104
    reference: chr 1
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.351G>A
  hgvsp: ENST00000533654.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.517G>A
  hgvsp: ENSP00000324074.8:p.Glu173Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.121G>A
  hgvsp: ENSP00000358112.4:p.Glu41Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.121G>A
  hgvsp: ENSP00000358111.2:p.Glu41Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.394G>A
  hgvsp: ENSP00000393718.2:p.Glu132Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.151G>A
  hgvsp: ENSP00000436529.1:p.Glu51Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3538G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.373G>A
  hgvsp: ENSP00000358115.3:p.Glu125Lys
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14541
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4545
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu173Lys
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

1-150199121-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199121
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199121
    reference: chr 1
allele count: 1
allele frequency: 8.273351534706709e-6
allele num: 120870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.134A>T
  hgvsp: ENSP00000436529.1:p.Asp45Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.334A>T
  hgvsp: ENSP00000435215.1:p.Met112Leu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.500A>T
  hgvsp: ENSP00000324074.8:p.Asp167Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.104A>T
  hgvsp: ENSP00000358112.4:p.Asp35Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.104A>T
  hgvsp: ENSP00000358111.2:p.Asp35Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3555A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.377A>T
  hgvsp: ENSP00000393718.2:p.Asp126Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.356A>T
  hgvsp: ENSP00000358115.3:p.Asp119Val
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10352
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4298
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3661
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp167Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

1-150199122-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199122
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199122
    reference: chr 1
allele count: 1
allele frequency: 8.274720728175424e-6
allele num: 120850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.333G>A
  hgvsp: ENST00000533654.1:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.103G>A
  hgvsp: ENSP00000358111.2:p.Asp35Asn
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3556G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.103G>A
  hgvsp: ENSP00000358112.4:p.Asp35Asn
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.133G>A
  hgvsp: ENSP00000436529.1:p.Asp45Asn
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.355G>A
  hgvsp: ENSP00000358115.3:p.Asp119Asn
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.499G>A
  hgvsp: ENSP00000324074.8:p.Asp167Asn
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.376G>A
  hgvsp: ENSP00000393718.2:p.Asp126Asn
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6282
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2917
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp167Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD

1-150199123-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199123
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199123
    reference: chr 1
allele count: 55528
allele frequency: 4.618788574470563e-1
allele num: 120222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3557C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.132C>A
  hgvsp: ENST00000534220.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.354C>A
  hgvsp: ENST00000369119.3:c.354C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.332C>A
  hgvsp: ENSP00000435215.1:p.Ala111Glu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.102C>A
  hgvsp: ENST00000369115.2:c.102C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.375C>A
  hgvsp: ENST00000436748.2:c.375C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.102C>A
  hgvsp: ENST00000369116.4:c.102C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.498C>A
  hgvsp: ENST00000314136.8:c.498C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.25e1
  variant carriers: 349
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.75e1
  variant carriers: 691
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 5.75e1
  variant carriers: 1460
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 421
genotype depth: GenotypeDepth
  all individuals: 13075
  bin: 2.75e1
  variant carriers: 5423
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 3.75e1
  variant carriers: 6339
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.25e1
  variant carriers: 252
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 8.75e1
  variant carriers: 322
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 2.25e1
  variant carriers: 3275
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 4.75e1
  variant carriers: 3572
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.25e1
  variant carriers: 537
genotype depth: GenotypeDepth
  all individuals: 10056
  bin: 3.25e1
  variant carriers: 6652
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 1.75e1
  variant carriers: 1310
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 5.25e1
  variant carriers: 2296
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 353
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 6.25e1
  variant carriers: 1017
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 9.75e1
  variant carriers: 2874
genotype depth: GenotypeDepth
  all individuals: 5704
  bin: 4.25e1
  variant carriers: 5041
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 4.75e1
  variant carriers: 253
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 47
genotype quality: GenotypeQuality
  all individuals: 3032
  bin: 6.75e1
  variant carriers: 619
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 4.25e1
  variant carriers: 144
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 8.25e1
  variant carriers: 835
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.5e0
  variant carriers: 35
hgvs: p.Ala111Glu
num of homozygotes: 13527
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

1-150199123-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199123
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199123
    reference: chr 1
allele count: 1
allele frequency: 8.317945134833891e-6
allele num: 120222
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.498C>T
  hgvsp: ENST00000314136.8:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.132C>T
  hgvsp: ENST00000534220.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.375C>T
  hgvsp: ENST00000436748.2:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.354C>T
  hgvsp: ENST00000369119.3:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.332C>T
  hgvsp: ENSP00000435215.1:p.Ala111Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3557C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.102C>T
  hgvsp: ENST00000369115.2:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.102C>T
  hgvsp: ENST00000369116.4:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10056
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10063
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala111Val
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

1-150199138-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199138
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199138
    reference: chr 1
allele count: 1
allele frequency: 8.578242146619315e-6
allele num: 116574
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3572A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.128-11A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.350-11A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.371-11A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.98-11A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.494-11A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.98-11A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.328-11A>T
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6086
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2283
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1790
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

1-150199140-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199140
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199141
    reference: chr 1
allele count: 1
allele frequency: 8.624407072013798e-6
allele num: 115950
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.98-14dupA
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.128-14dupA
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3575dupA
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.350-14dupA
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.371-14dupA
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.494-14dupA
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.98-14dupA
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.328-14dupA
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6075
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5933
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2196
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-150199141-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199141
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199141
    reference: chr 1
allele count: 1
allele frequency: 8.622324923692425e-6
allele num: 115978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3575A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.98-14A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.350-14A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.371-14A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.494-14A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.128-14A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.328-14A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.98-14A>G
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11002
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1833
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1930
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

1-150199160-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199160
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199160
    reference: chr 1
allele count: 1
allele frequency: 8.796776860958145e-6
allele num: 113678
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.494-33G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.98-33G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3594G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.371-33G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.328-33G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.128-33G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.350-33G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.98-33G>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9412
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5962
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4997
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3776
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7554
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1884
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16564
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

1-150199161-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199161
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199161
    reference: chr 1
allele count: 1
allele frequency: 8.805762490974094e-6
allele num: 113562
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.128-34A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.350-34A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.98-34A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.328-34A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.371-34A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3595A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.494-34A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.98-34A>C
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11395
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1397
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5298
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2134
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15180
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

1-150199178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199178
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199178
    reference: chr 1
allele count: 4
allele frequency: 3.617290649303671e-5
allele num: 110580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.350-51G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3612G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.328-51G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.98-51G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.494-51G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.128-51G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.371-51G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.98-51G>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10817
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13411
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6352
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6127
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5945
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

1-150199179-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150199179
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150199179
    reference: chr 1
allele count: 1
allele frequency: 9.037832366285271e-6
allele num: 110646
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.350-52A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.328-52A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.371-52A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.494-52A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.328-3613A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.128-52A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.98-52A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.98-52A>C
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3801
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6339
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5081
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

1-150201355-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201355
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201355
    reference: chr 1
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1551T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.493+50T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.97+50T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.349+50T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1551T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.97+50T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.370+50T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.127+50T>C
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46714
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7709
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
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: A
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

1-150201363-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201363
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201363
    reference: chr 1
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.493+42C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.349+42C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1543C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.370+42C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.127+42C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1543C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.97+42C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.97+42C>T
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

1-150201376-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201376
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201376
    reference: chr 1
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1530T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.127+29T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.97+29T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.349+29T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1530T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.97+29T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.493+29T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.370+29T>C
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1694
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS

1-150201379-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201379
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201379
    reference: chr 1
allele count: 2
allele frequency: 1.64883180266781e-5
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.349+26G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1527G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.493+26G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.370+26G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.97+26G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1527G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.127+26G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.97+26G>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7700
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

1-150201389-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201389
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201389
    reference: chr 1
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.127+16A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.493+16A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.97+16A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.97+16A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.370+16A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1517A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1517A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.349+16A>T
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

1-150201391-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201391
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201391
    reference: chr 1
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.493+14A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.370+14A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.127+14A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.97+14A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1515A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1515A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.97+14A>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.349+14A>C
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

1-150201398-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201398
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201398
    reference: chr 1
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.127+7G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.97+7G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1508G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.493+7G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1508G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.370+7G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.349+7G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.97+7G>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1751
  bin: 7.25e1
  variant carriers: 0
hgvs: c.493+7G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

1-150201399-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201399
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201399
    reference: chr 1
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1507C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.97+6C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.349+6C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1507C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.370+6C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.97+6C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.493+6C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.127+6C>T
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1752
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: c.493+6C>T
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

1-150201399-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201399
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201399
    reference: chr 1
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.493+6C>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.127+6C>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.370+6C>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1507C>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.97+6C>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.349+6C>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.97+6C>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1507C>G
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1752
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: c.493+6C>G
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

1-150201399-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201399
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201399
    reference: chr 1
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.493+6C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.97+6C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.127+6C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.97+6C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.370+6C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1507C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.349+6C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1507C>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: c.493+6C>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

1-150201406-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201406
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201406
    reference: chr 1
allele count: 6
allele frequency: 4.943886883868097e-5
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.492G>A
  hgvsp: ENST00000314136.8:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.96G>A
  hgvsp: ENST00000369115.2:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1500G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.96G>A
  hgvsp: ENST00000369116.4:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.342G>A
  hgvsp: ENST00000532744.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.126G>A
  hgvsp: ENST00000534220.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1500G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.348G>A
  hgvsp: ENST00000369119.3:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.369G>A
  hgvsp: ENST00000436748.2:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: c.492G>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/1-150201412-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201412
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201412
    reference: chr 1
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.90T>G
  hgvsp: ENSP00000358112.4:p.Asp30Glu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1494T>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.336T>G
  hgvsp: ENSP00000432684.1:p.Asp112Glu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1494T>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.90T>G
  hgvsp: ENSP00000358111.2:p.Asp30Glu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.363T>G
  hgvsp: ENSP00000393718.2:p.Asp121Glu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.120T>G
  hgvsp: ENSP00000436529.1:p.Asp40Glu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.486T>G
  hgvsp: ENSP00000324074.8:p.Asp162Glu
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.342T>G
  hgvsp: ENSP00000358115.3:p.Asp114Glu
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7718
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp162Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

1-150201412-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201412
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201412
    reference: chr 1
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.90T>C
  hgvsp: ENST00000369115.2:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.90T>C
  hgvsp: ENST00000369116.4:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.363T>C
  hgvsp: ENST00000436748.2:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.336T>C
  hgvsp: ENST00000532744.1:c.336T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1494T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.120T>C
  hgvsp: ENST00000534220.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.486T>C
  hgvsp: ENST00000314136.8:c.486T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1494T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.342T>C
  hgvsp: ENST00000369119.3:c.342T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9633
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47623
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1755
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp162Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

1-150201419-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201419
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201419
    reference: chr 1
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.479A>T
  hgvsp: ENSP00000324074.8:p.Glu160Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.356A>T
  hgvsp: ENSP00000393718.2:p.Glu119Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.335A>T
  hgvsp: ENSP00000358115.3:p.Glu112Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.83A>T
  hgvsp: ENSP00000358112.4:p.Glu28Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.83A>T
  hgvsp: ENSP00000358111.2:p.Glu28Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1487A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.329A>T
  hgvsp: ENSP00000432684.1:p.Glu110Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1487A>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.113A>T
  hgvsp: ENSP00000436529.1:p.Glu38Val
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu160Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

1-150201430-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201430
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201430
    reference: chr 1
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.72G>A
  hgvsp: ENST00000369115.2:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.102G>A
  hgvsp: ENST00000534220.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.72G>A
  hgvsp: ENST00000369116.4:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.345G>A
  hgvsp: ENST00000436748.2:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1476G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1476G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.468G>A
  hgvsp: ENST00000314136.8:c.468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.324G>A
  hgvsp: ENST00000369119.3:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.318G>A
  hgvsp: ENST00000532744.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32651
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro156Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/1-150201433-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201433
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201433
    reference: chr 1
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.99G>T
  hgvsp: ENST00000534220.1:c.99G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.465G>T
  hgvsp: ENST00000314136.8:c.465G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.342G>T
  hgvsp: ENST00000436748.2:c.342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.69G>T
  hgvsp: ENST00000369115.2:c.69G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.69G>T
  hgvsp: ENST00000369116.4:c.69G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1473G>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1473G>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.321G>T
  hgvsp: ENST00000369119.3:c.321G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.315G>T
  hgvsp: ENST00000532744.1:c.315G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala155Ala
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

1-150201460-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201460
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201460
    reference: chr 1
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.438T>C
  hgvsp: ENST00000314136.8:c.438T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.288T>C
  hgvsp: ENST00000532744.1:c.288T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.315T>C
  hgvsp: ENST00000436748.2:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.294T>C
  hgvsp: ENST00000369119.3:c.294T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1446T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.72T>C
  hgvsp: ENST00000534220.1:c.72T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-13T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1446T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-13T>C
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7717
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp146Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

1-150201474-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201474
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201474
    reference: chr 1
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.58A>G
  hgvsp: ENSP00000436529.1:p.Ile20Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.301A>G
  hgvsp: ENSP00000393718.2:p.Ile101Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.274A>G
  hgvsp: ENSP00000432684.1:p.Ile92Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.424A>G
  hgvsp: ENSP00000324074.8:p.Ile142Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-27A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1432A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1432A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.280A>G
  hgvsp: ENSP00000358115.3:p.Ile94Val
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-27A>G
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47605
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile142Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

1-150201478-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201478
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201478
    reference: chr 1
allele count: 82
allele frequency: 6.757313555830243e-4
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1428G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.276G>A
  hgvsp: ENST00000369119.3:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-31G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.297G>A
  hgvsp: ENST00000436748.2:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1428G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.270G>A
  hgvsp: ENST00000532744.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.420G>A
  hgvsp: ENST00000314136.8:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-31G>A
  variant of: http://identifiers.org/hgnc/16673
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 32659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: c.55-1G>A
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

1-150201497-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201497
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201497
    reference: chr 1
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.401G>A
  hgvsp: ENSP00000324074.8:p.Ser134Asn
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-20G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-50G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.251G>A
  hgvsp: ENSP00000432684.1:p.Ser84Asn
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.278G>A
  hgvsp: ENSP00000393718.2:p.Ser93Asn
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1409G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1409G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.257G>A
  hgvsp: ENSP00000358115.3:p.Ser86Asn
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-50G>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7677
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser134Asn
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-150201508-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201508
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201508
    reference: chr 1
allele count: 1
allele frequency: 8.265829062654984e-6
allele num: 120980
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.246T>C
  hgvsp: ENST00000369119.3:c.246T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-31T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1398T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-61T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-61T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1398T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.240T>C
  hgvsp: ENST00000532744.1:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.267T>C
  hgvsp: ENST00000436748.2:c.267T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.390T>C
  hgvsp: ENST00000314136.8:c.390T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47282
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp130Asp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

1-150201521-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201521
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201521
    reference: chr 1
allele count: 1
allele frequency: 8.292011476143882e-6
allele num: 120598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.227C>G
  hgvsp: ENSP00000432684.1:p.Thr76Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.377C>G
  hgvsp: ENSP00000324074.8:p.Thr126Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-74C>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-74C>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-44C>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.254C>G
  hgvsp: ENSP00000393718.2:p.Thr85Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.233C>G
  hgvsp: ENSP00000358115.3:p.Thr78Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1385C>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1385C>G
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr126Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-150201539-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201539
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201539
    reference: chr 1
allele count: 1
allele frequency: 8.428150021070375e-6
allele num: 118650
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.359T>G
  hgvsp: ENSP00000324074.8:p.Leu120Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1367T>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.236T>G
  hgvsp: ENSP00000393718.2:p.Leu79Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-92T>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1367T>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.209T>G
  hgvsp: ENSP00000432684.1:p.Leu70Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.215T>G
  hgvsp: ENSP00000358115.3:p.Leu72Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-62T>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-92T>G
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45635
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu120Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

1-150201559-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201559
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201559
    reference: chr 1
allele count: 1
allele frequency: 8.856140848064048e-6
allele num: 112916
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.189A>G
  hgvsp: ENST00000532744.1:c.189A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-82A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.195A>G
  hgvsp: ENST00000369119.3:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.339A>G
  hgvsp: ENST00000314136.8:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-112A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1347A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.216A>G
  hgvsp: ENST00000436748.2:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1347A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-112A>G
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys113Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

1-150201568-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201568
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201568
    reference: chr 1
allele count: 1
allele frequency: 9.117931323741269e-6
allele num: 109674
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.330A>G
  hgvsp: ENST00000314136.8:c.330A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-91A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.180A>G
  hgvsp: ENST00000532744.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1338A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.207A>G
  hgvsp: ENST00000436748.2:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1338A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.186A>G
  hgvsp: ENST00000369119.3:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-121A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-121A>G
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14634
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11017
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 3.25e1
  variant carriers: 0
hgvs: c.330A>G
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum

1-150201579-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201579
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201579
    reference: chr 1
allele count: 1
allele frequency: 9.670805771536885e-6
allele num: 103404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-102C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.184-9C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.328-9C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1327C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.178-9C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.205-9C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-132C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-132C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1327C>T
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14902
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20760
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28923
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-150201584-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201584
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201584
    reference: chr 1
allele count: 1
allele frequency: 9.879470460383324e-6
allele num: 101220
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.328-14C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1322C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.205-14C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-137C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1322C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-107C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.184-14C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.178-14C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-137C>T
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2736
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

1-150201599-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201599
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201599
    reference: chr 1
allele count: 3
allele frequency: 3.202049311559398e-5
allele num: 93690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-122G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1307G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.205-29G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.178-29G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.328-29G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1307G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-152G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.184-29G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-152G>C
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9895
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4596
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8697
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35685
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-150201602-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201602
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201602
    reference: chr 1
allele count: 1
allele frequency: 1.115274803711635e-5
allele num: 89664
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.328-32C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.178-32C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1304C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-155C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.205-32C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-155C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1304C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.184-32C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-125C>T
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28599
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6292
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

1-150201614-CATGTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201614
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201609
    reference: chr 1
allele count: 1
allele frequency: 1.734966515146258e-5
allele num: 57638
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.205-49_205-45delAACAT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-172_55-168delAACAT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.178-49_178-45delAACAT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.328-49_328-45delAACAT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-142_55-138delAACAT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1287_327+1291delAACAT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.184-49_184-45delAACAT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-172_55-168delAACAT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1287_327+1291delAACAT
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8643
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18683
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: CATGTT
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

1-150201616-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201616
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201615
    reference: chr 1
allele count: 2
allele frequency: 4.150066401062417e-5
allele num: 48192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.184-47delC
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1289delC
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.328-47delC
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.178-47delC
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-140delC
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.205-47delC
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-170delC
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1289delC
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-170delC
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17738
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5004
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4412
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20467
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: TG
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

1-150201617-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201617
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201617
    reference: chr 1
allele count: 1
allele frequency: 2.432261516758282e-5
allele num: 41114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.184-47C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-140C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.178-47C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.328-47C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1289C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1289C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.205-47C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-170C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-170C>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7531
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20048
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5777
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

1-150201619-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201619
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201619
    reference: chr 1
allele count: 1
allele frequency: 2.637687275796581e-5
allele num: 37912
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-172A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1287A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1287A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.184-49A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-142A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-172A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.328-49A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.205-49A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.178-49A>G
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3237
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7040
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

1-150201619-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201619
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201618
    reference: chr 1
allele count: 7
allele frequency: 1.846381093057607e-4
allele num: 37912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-173delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.328-50delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-173delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.178-50delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.205-50delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1286delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.184-50delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-143delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1286delT
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17476
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3237
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2894
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: TA
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

1-150201620-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150201620
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150201620
    reference: chr 1
allele count: 7
allele frequency: 4.1351606805293e-4
allele num: 16928
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.328-50T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-173T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.205-50T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-143T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.184-50T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.178-50T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.327+1286T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-173T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.327+1286T>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23461
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17701
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2628
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5866
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17251
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23704
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

1-150202911-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150202911
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150202911
    reference: chr 1
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.322G>C
  hgvsp: ENSP00000435215.1:p.Ala108Pro
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.178G>C
  hgvsp: ENSP00000358115.3:p.Ala60Pro
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.172G>C
  hgvsp: ENSP00000432684.1:p.Ala58Pro
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1464G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.322G>C
  hgvsp: ENSP00000358110.5:p.Ala108Pro
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1204G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1464G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.322G>C
  hgvsp: ENSP00000324074.8:p.Ala108Pro
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1434G>C
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1302
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29864
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala108Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD

1-150202920-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150202920
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150202920
    reference: chr 1
allele count: 3
allele frequency: 2.475410918212423e-5
allele num: 121192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1443A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.313A>G
  hgvsp: ENSP00000435215.1:p.Thr105Ala
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.163A>G
  hgvsp: ENSP00000432684.1:p.Thr55Ala
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.169A>G
  hgvsp: ENSP00000358115.3:p.Thr57Ala
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.313A>G
  hgvsp: ENSP00000324074.8:p.Thr105Ala
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1473A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1473A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1195A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.313A>G
  hgvsp: ENSP00000358110.5:p.Thr105Ala
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29913
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7962
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3075
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr105Ala
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-150202921-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150202921
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150202921
    reference: chr 1
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.312T>G
  hgvsp: ENSP00000358110.5:p.Ser104Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1444T>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.312T>G
  hgvsp: ENSP00000324074.8:p.Ser104Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1474T>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.312T>G
  hgvsp: ENSP00000435215.1:p.Ser104Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1194T>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.162T>G
  hgvsp: ENSP00000432684.1:p.Ser54Arg
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1474T>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.168T>G
  hgvsp: ENSP00000358115.3:p.Ser56Arg
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2885
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7959
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser104Arg
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

1-150202939-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150202939
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150202939
    reference: chr 1
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.294C>A
  hgvsp: ENSP00000358110.5:p.Asn98Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.294C>A
  hgvsp: ENSP00000324074.8:p.Asn98Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1462C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1492C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.150C>A
  hgvsp: ENSP00000358115.3:p.Asn50Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.144C>A
  hgvsp: ENSP00000432684.1:p.Asn48Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.294C>A
  hgvsp: ENSP00000435215.1:p.Asn98Lys
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1492C>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1176C>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29998
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn98Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

1-150202946-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150202946
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150202946
    reference: chr 1
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.287G>C
  hgvsp: ENSP00000358110.5:p.Ser96Thr
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1169G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1469G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.287G>C
  hgvsp: ENSP00000435215.1:p.Ser96Thr
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.137G>C
  hgvsp: ENSP00000432684.1:p.Ser46Thr
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.287G>C
  hgvsp: ENSP00000324074.8:p.Ser96Thr
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1499G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.143G>C
  hgvsp: ENSP00000358115.3:p.Ser48Thr
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1499G>C
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3073
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser96Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

1-150202978-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150202978
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150202978
    reference: chr 1
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.255G>A
  hgvsp: ENST00000369114.5:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1531G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.111G>A
  hgvsp: ENST00000369119.3:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.255G>A
  hgvsp: ENST00000314136.8:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1531G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1501G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.105G>A
  hgvsp: ENST00000532744.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.255G>A
  hgvsp: ENST00000533654.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1137G>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1858
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7958
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Glu85Glu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

1-150202980-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150202980
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150202980
    reference: chr 1
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.109G>C
  hgvsp: ENSP00000358115.3:p.Glu37Gln
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1533G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1503G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1135G>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.253G>C
  hgvsp: ENSP00000435215.1:p.Glu85Gln
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.253G>C
  hgvsp: ENSP00000324074.8:p.Glu85Gln
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.103G>C
  hgvsp: ENSP00000432684.1:p.Glu35Gln
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.253G>C
  hgvsp: ENSP00000358110.5:p.Glu85Gln
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1533G>C
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11163
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29984
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2889
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu85Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

1-150202986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150202986
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150202986
    reference: chr 1
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.97C>T
  hgvsp: ENST00000532744.1:c.97C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.103C>T
  hgvsp: ENST00000369119.3:c.103C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1539C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.247C>T
  hgvsp: ENST00000314136.8:c.247C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.247C>T
  hgvsp: ENST00000533654.1:c.247C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1539C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.247C>T
  hgvsp: ENST00000369114.5:c.247C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1129C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1509C>T
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3073
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2888
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3965
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu83Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

1-150203028-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150203028
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150203028
    reference: chr 1
allele count: 15
allele frequency: 1.240345973836969e-4
allele num: 120934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1087T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.61T>C
  hgvsp: ENST00000369119.3:c.61T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.55T>C
  hgvsp: ENST00000532744.1:c.55T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.205T>C
  hgvsp: ENST00000369114.5:c.205T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.205T>C
  hgvsp: ENST00000533654.1:c.205T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1581T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.205T>C
  hgvsp: ENST00000314136.8:c.205T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1551T>C
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1581T>C
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9969
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3956
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
hgvs: c.205T>C
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

1-150203032-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150203032
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150203032
    reference: chr 1
allele count: 1
allele frequency: 8.271572260455268e-6
allele num: 120896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.205-4A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.205-4A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1555A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.55-4A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1585A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1083A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.205-4A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1585A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.61-4A>G
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
hgvs: c.205-4A>G
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

1-150203036-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150203036
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150203036
    reference: chr 1
allele count: 1
allele frequency: 8.274036074797286e-6
allele num: 120860
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1559A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1589A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.61-8A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.55-8A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.205-8A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1079A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.205-8A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.205-8A>G
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1589A>G
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3049
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3955
  bin: 7.75e1
  variant carriers: 0
hgvs: c.205-8A>G
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

1-150203046-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150203046
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150203047
    reference: chr 1
allele count: 1
allele frequency: 8.284866862189524e-6
allele num: 120702
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.205-19dupT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1600dupT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.61-19dupT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1600dupT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.205-19dupT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.55-19dupT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1570dupT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.205-19dupT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1068dupT
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

1-150203046-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150203046
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150203045
    reference: chr 1
allele count: 1
allele frequency: 8.284866862189524e-6
allele num: 120702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1600delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.205-19delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.205-19delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1570delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1600delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.61-19delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.55-19delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1068delT
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.205-19delT
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9111
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7946
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3937
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: GA
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

1-150203054-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150203054
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150203054
    reference: chr 1
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.205-26G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1061G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.205-26G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.205-26G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1577G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1607G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1607G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.61-26G>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.55-26G>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28062
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1852
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

1-150203056-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150203056
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150203056
    reference: chr 1
allele count: 4
allele frequency: 3.317299718029524e-5
allele num: 120580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1609T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1579T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.205-28T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.61-28T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.55-28T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.205-28T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1059T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.205-28T>A
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1609T>A
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2991
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2870
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9156
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

1-150203068-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 150203068
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 150203068
    reference: chr 1
allele count: 1
allele frequency: 8.360225391676559e-6
allele num: 119614
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000324074
  ensembl transcript: ENST00000314136
  gene symbol: ANP32E
  hgvsc: ENST00000314136.8:c.205-40C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000435215
  ensembl transcript: ENST00000533654
  gene symbol: ANP32E
  hgvsc: ENST00000533654.1:c.205-40C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000436529
  ensembl transcript: ENST00000534220
  gene symbol: ANP32E
  hgvsc: ENST00000534220.1:c.55-1591C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358110
  ensembl transcript: ENST00000369114
  gene symbol: ANP32E
  hgvsc: ENST00000369114.5:c.205-40C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000393718
  ensembl transcript: ENST00000436748
  gene symbol: ANP32E
  hgvsc: ENST00000436748.2:c.204+1047C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000432684
  ensembl transcript: ENST00000532744
  gene symbol: ANP32E
  hgvsc: ENST00000532744.1:c.55-40C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358115
  ensembl transcript: ENST00000369119
  gene symbol: ANP32E
  hgvsc: ENST00000369119.3:c.61-40C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358112
  ensembl transcript: ENST00000369116
  gene symbol: ANP32E
  hgvsc: ENST00000369116.4:c.55-1621C>T
  variant of: http://identifiers.org/hgnc/16673
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143401
  ensembl protein: ENSP00000358111
  ensembl transcript: ENST00000369115
  gene symbol: ANP32E
  hgvsc: ENST00000369115.2:c.55-1621C>T
  variant of: http://identifiers.org/hgnc/16673
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11100
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3573
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1576
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G

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

GenotypeQuality
all individuals: 7652
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17826
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 96
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4780
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2969
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.212415130940834e-4
allele num: 16496
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: 8630
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.316e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: 5.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

DP
type: SiteQuality
SIO_000300: 2.667614e6

GenotypeQuality
all individuals: 4743
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7576
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2938
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17793
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17494
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.879e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.822e0

DP
type: SiteQuality
SIO_000300: 2.658923e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

QD
type: SiteQuality
SIO_000300: 1.432e1

MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

FS
type: SiteQuality
SIO_000300: 4.707e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.503e-1

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3363
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17508
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2930
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.628e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.098e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 7.81e0

DP
type: SiteQuality
SIO_000300: 2.654732e6

QD
type: SiteQuality
SIO_000300: 2.816e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.41e-1

GenotypeQuality
all individuals: 2930
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7551
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 111
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3819
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3357
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17792
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 17480
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
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: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.118e0

QD
type: SiteQuality
SIO_000300: 2.316e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-2

DP
type: SiteQuality
SIO_000300: 2.653805e6

FS
type: SiteQuality
SIO_000300: 3.425e0

MQ
type: SiteQuality
SIO_000300: 5.9e1

MQRankSum
type: SiteQuality
SIO_000300: -1.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.832000000000001e-1

GenotypeQuality
all individuals: 159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2913
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7482
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17438
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4690
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3787
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003273568189326e-5
allele num: 66594
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.817883985353633e-4
allele num: 10378
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212856276531231e-4
allele num: 16490
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

FS
type: SiteQuality
SIO_000300: 2.868e0

VQSLOD
type: SiteQuality
SIO_000300: 2.7e-1

DP
type: SiteQuality
SIO_000300: 2.65289e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-1

QD
type: SiteQuality
SIO_000300: 2.989e1

MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeQuality
all individuals: 17734
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2901
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
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variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7290
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.593e0

MQRankSum
type: SiteQuality
SIO_000300: -1.416e0

VQSLOD
type: SiteQuality
SIO_000300: -4.378e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.651e0

DP
type: SiteQuality
SIO_000300: 2.633299e6

FS
type: SiteQuality
SIO_000300: 6.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.56e-1

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

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

GenotypeQuality
all individuals: 1923
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7277
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4578
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variant carriers: 0

GenotypeQuality
all individuals: 353
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 3736
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 211
bin: 4.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.67e-1

MQ
type: SiteQuality
SIO_000300: 6.19e1

MQRankSum
type: SiteQuality
SIO_000300: 2.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.382e0

VQSLOD
type: SiteQuality
SIO_000300: -1.58e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-2

QD
type: SiteQuality
SIO_000300: 1.962e1

DP
type: SiteQuality
SIO_000300: 2.63253e6

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

GenotypeQuality
all individuals: 17724
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 246
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1920
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GenotypeQuality
all individuals: 2900
bin: 9.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3213
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17131
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7277
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.809e0

MQ
type: SiteQuality
SIO_000300: 6.116e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-2

DP
type: SiteQuality
SIO_000300: 2.629855e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

QD
type: SiteQuality
SIO_000300: 5.6e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.753e0

GenotypeQuality
all individuals: 1587
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66382
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.933e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

FS
type: SiteQuality
SIO_000300: 5.281e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.086e0

DP
type: SiteQuality
SIO_000300: 2.601199e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.37e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.409999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 5.705e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.424e0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506704836522525e-5
allele num: 66370
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.92e-1

FS
type: SiteQuality
SIO_000300: 1.745e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.888e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.43e-2

DP
type: SiteQuality
SIO_000300: 2.601461e6

MQ
type: SiteQuality
SIO_000300: 5.847e1

QD
type: SiteQuality
SIO_000300: 8.02e0

GenotypeQuality
all individuals: 10063
bin: 6.25e1
variant carriers: 498

GenotypeQuality
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variant carriers: 469

GenotypeQuality
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variant carriers: 852

GenotypeQuality
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GenotypeQuality
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variant carriers: 57

GenotypeQuality
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variant carriers: 268

GenotypeQuality
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variant carriers: 55

GenotypeQuality
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GenotypeQuality
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variant carriers: 201

GenotypeQuality
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variant carriers: 404

GenotypeQuality
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variant carriers: 380

GenotypeQuality
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variant carriers: 36061

GenotypeQuality
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variant carriers: 126

GenotypeQuality
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bin: 7.75e1
variant carriers: 769

East Asian
type: Population
allele count: 4216
allele frequency: 4.92063492063492e-1
allele num: 8568
num of homozygotes: 1031

South Asian
type: Population
allele count: 7309
allele frequency: 4.469789628180039e-1
allele num: 16352
num of homozygotes: 1658

Latino
type: Population
allele count: 5109
allele frequency: 4.464348130024467e-1
allele num: 11444
num of homozygotes: 1136

Other
type: Population
allele count: 385
allele frequency: 4.306487695749441e-1
allele num: 894
num of homozygotes: 83

European (Finnish)
type: Population
allele count: 2604
allele frequency: 3.963470319634703e-1
allele num: 6570
num of homozygotes: 493

African
type: Population
allele count: 8766
allele frequency: 8.454861111111112e-1
allele num: 10368
num of homozygotes: 3715

European (Non-Finnish)
type: Population
allele count: 27139
allele frequency: 4.110350467997456e-1
allele num: 66026
num of homozygotes: 5411

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.41e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-2

QD
type: SiteQuality
SIO_000300: 1.922e1

FS
type: SiteQuality
SIO_000300: 1.951e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.23e-1

DP
type: SiteQuality
SIO_000300: 2.632579e6

MQ
type: SiteQuality
SIO_000300: 5.883e1

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 272
bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514554872323024e-5
allele num: 66026
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16352
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.632579e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

QD
type: SiteQuality
SIO_000300: 1.922e1

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.41e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-2

FS
type: SiteQuality
SIO_000300: 1.951e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.23e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.958175662218681e-5
allele num: 10042
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64340
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

DP
type: SiteQuality
SIO_000300: 1.788668e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 1.199e1

FS
type: SiteQuality
SIO_000300: 3.291e0

MQRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1428
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.146788990825688e-3
allele num: 872
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14740
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.882e1

QD
type: SiteQuality
SIO_000300: 7.48e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 1.768831e6

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

FS
type: SiteQuality
SIO_000300: 4.448e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-1

GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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: 14786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558700667123886e-5
allele num: 64156
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

DP
type: SiteQuality
SIO_000300: 1.760149e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

FS
type: SiteQuality
SIO_000300: 4.491e0

QD
type: SiteQuality
SIO_000300: 1.525e1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.204238921001927e-4
allele num: 8304
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11236
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: 6478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63242
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.77e0

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 3.294e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.637e0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13620
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.744e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.590839e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.75e-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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variant carriers: 0

GenotypeQuality
all individuals: 3461
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.227784771311449e-5
allele num: 61962
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8174
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.601794009290405e-4
allele num: 12486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

FS
type: SiteQuality
SIO_000300: 8.125e0

MQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

VQSLOD
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SIO_000300: -1.216e0

ReadPosRankSum
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SIO_000300: -1.04e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

QD
type: SiteQuality
SIO_000300: 1.004e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

DP
type: SiteQuality
SIO_000300: 1.546764e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.029442042413012e-4
allele num: 9714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10982
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62018
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12492
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.623e0

MQ
type: SiteQuality
SIO_000300: 5.832e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.089e0

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.727e0

DP
type: SiteQuality
SIO_000300: 1.548007e6

QD
type: SiteQuality
SIO_000300: 1.995e1

VQSLOD
type: SiteQuality
SIO_000300: -1.718e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
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: 10354
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

FS
type: SiteQuality
SIO_000300: 4.814e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.05e-1

QD
type: SiteQuality
SIO_000300: 8.99e0

DP
type: SiteQuality
SIO_000300: 1.667709e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-2

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 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: 10356
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.34e-1

DP
type: SiteQuality
SIO_000300: 1.668644e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.301e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 228
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GenotypeQuality
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variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

MQ
type: SiteQuality
SIO_000300: 5.898e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: -1.356e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.555e0

DP
type: SiteQuality
SIO_000300: 1.670108e6

QD
type: SiteQuality
SIO_000300: 1.58e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 8.779999999999999e0

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 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: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998860433035446e-5
allele num: 66692
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.45e-1

QD
type: SiteQuality
SIO_000300: 1.009e1

BaseQRankSum
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SIO_000300: -3.046e0

DP
type: SiteQuality
SIO_000300: 1.670451e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

FS
type: SiteQuality
SIO_000300: 2.156e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.08e-1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.04e0

DP
type: SiteQuality
SIO_000300: 1.671433e6

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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MQRankSum
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.369999999999999e0

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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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
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num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 7.64e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
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Other
type: Population
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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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African
type: Population
allele count: 0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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African
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Latino
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European (Non-Finnish)
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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BaseQRankSum
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QD
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DP
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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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European (Finnish)
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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South Asian
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African
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European (Non-Finnish)
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BaseQRankSum
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DP
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QD
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VQSLOD
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ReadPosRankSum
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MQ
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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Latino
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FS
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QD
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ReadPosRankSum
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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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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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Latino
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European (Finnish)
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South Asian
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Other
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African
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European (Non-Finnish)
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allele frequency: 7.494004796163069e-5
allele num: 66720
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East Asian
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VQSLOD
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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QD
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FS
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ClippingRankSum
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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East Asian
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African
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Latino
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South Asian
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European (Non-Finnish)
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DP
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VQSLOD
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BaseQRankSum
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QD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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African
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European (Finnish)
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BaseQRankSum
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MQRankSum
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FS
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MQ
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QD
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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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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East Asian
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European (Non-Finnish)
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South Asian
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Latino
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African
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European (Finnish)
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Other
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InbreedingCoeff
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MQ
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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MQ
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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Other
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European (Non-Finnish)
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VQSLOD
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MQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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QD
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ClippingRankSum
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FS
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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South Asian
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allele frequency: 0.0e0
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Latino
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European (Finnish)
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East Asian
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African
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VQSLOD
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FS
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BaseQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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QD
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Other
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South Asian
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Latino
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European (Non-Finnish)
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African
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QD
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InbreedingCoeff
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MQ
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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allele num: 66714
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Other
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African
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South Asian
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allele frequency: 1.878332525448376e-3
allele num: 16504
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Latino
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allele frequency: 8.644536652835408e-5
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
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QD
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DP
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VQSLOD
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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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South Asian
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African
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allele frequency: 0.0e0
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Other
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.50105073551486e-5
allele num: 66620
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ReadPosRankSum
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FS
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VQSLOD
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MQRankSum
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BaseQRankSum
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MQ
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QD
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DP
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InbreedingCoeff
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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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European (Finnish)
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Other
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East Asian
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African
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European (Non-Finnish)
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Latino
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South Asian
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VQSLOD
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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DP
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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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European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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African
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East Asian
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South Asian
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VQSLOD
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BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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QD
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ClippingRankSum
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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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European (Finnish)
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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African
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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South Asian
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Latino
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African
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Other
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European (Finnish)
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MQRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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FS
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DP
type: SiteQuality
SIO_000300: 1.496082e6

VQSLOD
type: SiteQuality
SIO_000300: -8.757e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.683955274147919e-5
allele num: 59384
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

MQRankSum
type: SiteQuality
SIO_000300: -2.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.4212e6

QD
type: SiteQuality
SIO_000300: 1.367e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.798043728423475e-5
allele num: 55616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7380
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

DP
type: SiteQuality
SIO_000300: 1.234911e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

QD
type: SiteQuality
SIO_000300: 1.704e1

VQSLOD
type: SiteQuality
SIO_000300: 8.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.855e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8678
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.841010346478147e-5
allele num: 54318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7228
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.14682e6

VQSLOD
type: SiteQuality
SIO_000300: -2.567e0

QD
type: SiteQuality
SIO_000300: 2.638e1

FS
type: SiteQuality
SIO_000300: 1.481e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.755e0

MQRankSum
type: SiteQuality
SIO_000300: -1.037e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.16e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 87
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.476275738585497e-4
allele num: 6702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49962
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.462e0

QD
type: SiteQuality
SIO_000300: 1.115e1

FS
type: SiteQuality
SIO_000300: 9.19e0

MQRankSum
type: SiteQuality
SIO_000300: -5.41e-1

DP
type: SiteQuality
SIO_000300: 9.06683e5

VQSLOD
type: SiteQuality
SIO_000300: -1.49e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47764
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.272912423625254e-4
allele num: 7856
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5330
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.261e0

MQ
type: SiteQuality
SIO_000300: 5.927e1

DP
type: SiteQuality
SIO_000300: 8.68566e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: -2.073e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.51e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.223e0

QD
type: SiteQuality
SIO_000300: 8.960000000000001e0

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: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4564
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.287282708142727e-4
allele num: 4372
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8682
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5266
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.814e1

DP
type: SiteQuality
SIO_000300: 7.06105e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.57e-2

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.07e0

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.612330198537095e-4
allele num: 3828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7364
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.956635277360133e-5
allele num: 25274
num of homozygotes: 0

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.845e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.24e-1

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.282e0

MQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

DP
type: SiteQuality
SIO_000300: 6.86406e5

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22228
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.413127413127413e-4
allele num: 4144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2770
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 6.81794e5

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.159e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.211e0

QD
type: SiteQuality
SIO_000300: 1.341e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 111
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.747252747252747e-4
allele num: 3640
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5866
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 6.66927e5

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

FS
type: SiteQuality
SIO_000300: 5.815e0

VQSLOD
type: SiteQuality
SIO_000300: 4.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.91e-2

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 2.747252747252747e-4
allele num: 3640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 1.243781094527363e-3
allele num: 3216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.045408678102926e-5
allele num: 19820
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2414
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.840245775729647e-4
allele num: 2604
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.91e-2

DP
type: SiteQuality
SIO_000300: 6.66927e5

MQRankSum
type: SiteQuality
SIO_000300: -8.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

FS
type: SiteQuality
SIO_000300: 5.815e0

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6

European (Non-Finnish)
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allele count: 3
allele frequency: 2.98804780876494e-4
allele num: 10040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1778
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 5.370569280343716e-4
allele num: 1862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 2.586206896551724e-3
allele num: 1160
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1120
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.313e0

MQ
type: SiteQuality
SIO_000300: 5.871e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.735e0

MQRankSum
type: SiteQuality
SIO_000300: -5.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 9.51e0

DP
type: SiteQuality
SIO_000300: 6.63961e5

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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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

QD
type: SiteQuality
SIO_000300: 1.427e1

MQ
type: SiteQuality
SIO_000300: 5.913e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.02e-1

DP
type: SiteQuality
SIO_000300: 2.416691e6

VQSLOD
type: SiteQuality
SIO_000300: 5.0e-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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bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.819725827975252e-4
allele num: 16486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

VQSLOD
type: SiteQuality
SIO_000300: 5.28e-1

QD
type: SiteQuality
SIO_000300: 1.31e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.765e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

DP
type: SiteQuality
SIO_000300: 2.417842e6

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

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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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
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: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.413e1

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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bin: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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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
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.399e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.23e-1

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

FS
type: SiteQuality
SIO_000300: 8.895e0

MQ
type: SiteQuality
SIO_000300: 5.868e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

DP
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
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
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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DP
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SIO_000300: 2.419082e6

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

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

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

South Asian
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allele 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

ClippingRankSum
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
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FS
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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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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9452
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7958
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1858
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3971
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3074
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
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: 8650
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.419024e6

QD
type: SiteQuality
SIO_000300: 1.51e1

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

MQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.125e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9455
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1858
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7957
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29954
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

European (Finnish)
type: Population
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: 16492
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.126e1

DP
type: SiteQuality
SIO_000300: 2.418673e6

FS
type: SiteQuality
SIO_000300: 1.4266e1

MQ
type: SiteQuality
SIO_000300: 5.838e1

VQSLOD
type: SiteQuality
SIO_000300: -2.61e0

MQRankSum
type: SiteQuality
SIO_000300: -9.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.005e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.659e0

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

GenotypeQuality
all individuals: 9406
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29382
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7961
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 2881
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1858
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

East Asian
type: Population
allele count: 15
allele frequency: 1.740543049431423e-3
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.898e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

FS
type: SiteQuality
SIO_000300: 2.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.411816e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

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

GenotypeQuality
all individuals: 3053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1857
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7947
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3957
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9399
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2882
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29192
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
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: 1
allele frequency: 1.502900598154438e-5
allele num: 66538
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.409622e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e0

MQ
type: SiteQuality
SIO_000300: 5.804e1

QD
type: SiteQuality
SIO_000300: 1.634e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.845e0

VQSLOD
type: SiteQuality
SIO_000300: -2.021e0

MQRankSum
type: SiteQuality
SIO_000300: 7.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.75e-1

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29039
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 106
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9393
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7946
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
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: 8612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.332e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

FS
type: SiteQuality
SIO_000300: 1.965e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.56e0

VQSLOD
type: SiteQuality
SIO_000300: 4.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-2

DP
type: SiteQuality
SIO_000300: 2.408193e6

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

GenotypeQuality
all individuals: 1302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28767
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3032
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9342
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3937
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7946
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 9.865824782951855e-5
allele num: 10136
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

VQSLOD
type: SiteQuality
SIO_000300: 5.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

DP
type: SiteQuality
SIO_000300: 2.405632e6

QD
type: SiteQuality
SIO_000300: 1.174e1

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

GenotypeQuality
all individuals: 9342
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1048
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28767
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3032
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

QD
type: SiteQuality
SIO_000300: 1.174e1

MQRankSum
type: SiteQuality
SIO_000300: 6.03e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.25e0

DP
type: SiteQuality
SIO_000300: 2.405632e6

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2871
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1528
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3922
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3019
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7938
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9299
bin: 6.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66418
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.399573e6

VQSLOD
type: SiteQuality
SIO_000300: 4.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.761e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.25e-1

FS
type: SiteQuality
SIO_000300: 1.747e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 9.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3915
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7944
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2074
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1299
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1853
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27499
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.659832246039142e-4
allele num: 8584
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.15e0

FS
type: SiteQuality
SIO_000300: 3.651e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: -3.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

QD
type: SiteQuality
SIO_000300: 1.125e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.24e-1

DP
type: SiteQuality
SIO_000300: 2.391972e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.71e-1

GenotypeQuality
all individuals: 551
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4449
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6537
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2590
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8544
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24779
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2737
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65990
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.116956202593589e-5
allele num: 16348
num of homozygotes: 0