2-74682733-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682733
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682733
    reference: chr 2
allele count: 2
allele frequency: 1.715089356155456e-5
allele num: 116612
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+8C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+8C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+8C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-212C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+8C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+8C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+8C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+8C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+8C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+8C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+8C>G
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.251+8C>G
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-74682734-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682734
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682734
    reference: chr 2
allele count: 1
allele frequency: 8.575152637716951e-6
allele num: 116616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+9A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+9A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+9A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+9A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+9A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-211A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+9A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+9A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+9A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+9A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+9A>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

2-74682739-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682739
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682739
    reference: chr 2
allele count: 1
allele frequency: 8.612670961518585e-6
allele num: 116108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+14G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+14G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+14G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+14G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-206G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+14G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+14G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+14G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+14G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+14G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+14G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7625
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum

2-74682742-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682742
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682742
    reference: chr 2
allele count: 1
allele frequency: 8.638861052558831e-6
allele num: 115756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+17C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+17C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+17C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+17C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+17C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+17C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+17C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+17C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+17C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-203C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+17C>T
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

2-74682744-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682744
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682744
    reference: chr 2
allele count: 2
allele frequency: 1.72995415621486e-5
allele num: 115610
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-201T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+19T>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3584
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

2-74682746-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682746
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682746
    reference: chr 2
allele count: 1
allele frequency: 8.670921198668147e-6
allele num: 115328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+21G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+21G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+21G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+21G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+21G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+21G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+21G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-199G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+21G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+21G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+21G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS

2-74682754-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682754
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682755
    reference: chr 2
allele count: 1
allele frequency: 8.720524626761546e-6
allele num: 114672
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-187dupG
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+33dupG
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+33dupG
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+33dupG
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+33dupG
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+33dupG
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+33dupG
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+33dupG
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+33dupG
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+33dupG
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+33dupG
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

2-74682756-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682756
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682756
    reference: chr 2
allele count: 1
allele frequency: 8.75825465501235e-6
allele num: 114178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+31G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+31G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+31G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+31G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+31G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+31G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-189G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+31G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+31G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+31G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+31G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7625
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

2-74682758-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682758
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682758
    reference: chr 2
allele count: 1
allele frequency: 8.770083491194836e-6
allele num: 114024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+33G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+33G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+33G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+33G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-187G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+33G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+33G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+33G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+33G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+33G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+33G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3659
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-74682759-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682759
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682759
    reference: chr 2
allele count: 2
allele frequency: 1.753401599102258e-5
allele num: 114064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+34A>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+34A>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+34A>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+34A>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+34A>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+34A>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+34A>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+34A>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+34A>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+34A>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-186A>T
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7625
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2466
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

2-74682762-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682762
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682762
    reference: chr 2
allele count: 1
allele frequency: 8.797241185164333e-6
allele num: 113672
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+37T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+37T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+37T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+37T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+37T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+37T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+37T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+37T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-183T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+37T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+37T>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7625
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27426
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

2-74682765-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682765
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682765
    reference: chr 2
allele count: 1
allele frequency: 8.822854722874133e-6
allele num: 113342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-180A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+40A>G
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3666
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-74682767-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682767
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682767
    reference: chr 2
allele count: 1
allele frequency: 8.834234425244708e-6
allele num: 113196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+42G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+42G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+42G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+42G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+42G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+42G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+42G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+42G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+42G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-178G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+42G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6750
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2869
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

2-74682768-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682768
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682768
    reference: chr 2
allele count: 1
allele frequency: 8.843140376010329e-6
allele num: 113082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+43A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+43A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+43A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+43A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+43A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-177A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+43A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+43A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+43A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+43A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+43A>G
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6750
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3526
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

2-74682772-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682772
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682772
    reference: chr 2
allele count: 1
allele frequency: 8.854729310924966e-6
allele num: 112934
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.107+47G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.491+47G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.251+47G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.268+47G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.251+47G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.396+47G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.251+47G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.251+47G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-173G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.266+47G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.251+47G>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7630
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6750
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum

2-74682895-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682895
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682895
    reference: chr 2
allele count: 271
allele frequency: 2.249784153549844e-3
allele num: 120456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.108-50G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.267-50G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.252-50G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.492-50G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.252-50G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.252-50G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.252-50G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.252-50G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.397-50G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-50G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.269-34G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 8.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 9.75e1
  variant carriers: 193
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

2-74682905-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682905
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682905
    reference: chr 2
allele count: 2
allele frequency: 1.658869977771142e-5
allele num: 120564
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.397-40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.267-40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.252-40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.252-40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.492-40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.252-40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.108-40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.252-40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.269-24A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.252-40A>G
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

2-74682906-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682906
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682906
    reference: chr 2
allele count: 1
allele frequency: 8.298755186721992e-6
allele num: 120500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.269-23C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-39C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.108-39C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.252-39C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.252-39C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.252-39C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.492-39C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.397-39C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.252-39C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.252-39C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.267-39C>T
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4900
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46455
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

2-74682907-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682907
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682907
    reference: chr 2
allele count: 1
allele frequency: 8.293111741387604e-6
allele num: 120582
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.252-38G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-38G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.269-22G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.252-38G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.108-38G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.267-38G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.397-38G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.252-38G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.492-38G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.252-38G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.252-38G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/2-74682915-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682915
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682915
    reference: chr 2
allele count: 1
allele frequency: 8.276775368316504e-6
allele num: 120820
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.267-30A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.252-30A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.252-30A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.269-14A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-30A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.108-30A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.397-30A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.492-30A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.252-30A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.252-30A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.252-30A>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1339
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS

2-74682926-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682926
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682926
    reference: chr 2
allele count: 3
allele frequency: 2.478478544637399e-5
allele num: 121042
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.252-19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.269-3T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.397-19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.252-19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.252-19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.492-19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.267-19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.252-19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.108-19T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.252-19T>C
  variant of: http://identifiers.org/hgnc/13324
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.269-3T>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

2-74682935-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682935
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682935
    reference: chr 2
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.252-10T>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.275T>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.397-10T>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.252-10T>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.267-10T>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.252-10T>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.252-10T>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.252-10T>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.59-10T>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.492-10T>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.108-10T>G
  variant of: http://identifiers.org/hgnc/13324
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

2-74682948-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682948
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682948
    reference: chr 2
allele count: 3
allele frequency: 2.472839974282464e-5
allele num: 121318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.495T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.111T>C
  hgvsp: ENST00000455562.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.288T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.255T>C
  hgvsp: ENST00000441673.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.255T>C
  hgvsp: ENST00000431187.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.270T>C
  hgvsp: ENST00000409493.2:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.62T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.255T>C
  hgvsp: ENST00000452361.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.255T>C
  hgvsp: ENST00000409917.1:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.255T>C
  hgvsp: ENST00000233331.7:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.400T>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val85Val
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

2-74682952-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682952
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682952
    reference: chr 2
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.259A>G
  hgvsp: ENSP00000388677.1:p.Thr87Ala
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.259A>G
  hgvsp: ENSP00000387267.1:p.Thr87Ala
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.499A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.404A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.66A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.259A>G
  hgvsp: ENSP00000392498.1:p.Thr87Ala
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.274A>G
  hgvsp: ENSP00000386937.2:p.Thr92Ala
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.259A>G
  hgvsp: ENSP00000389887.1:p.Thr87Ala
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.115A>G
  hgvsp: ENSP00000398740.1:p.Thr39Ala
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.292A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.259A>G
  hgvsp: ENSP00000233331.7:p.Thr87Ala
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr87Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

2-74682954-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682954
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682954
    reference: chr 2
allele count: 5
allele frequency: 4.120313143798929e-5
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.261C>T
  hgvsp: ENST00000409917.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.261C>T
  hgvsp: ENST00000233331.7:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.117C>T
  hgvsp: ENST00000455562.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.261C>T
  hgvsp: ENST00000441673.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.501C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.261C>T
  hgvsp: ENST00000452361.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.406C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.261C>T
  hgvsp: ENST00000431187.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.276C>T
  hgvsp: ENST00000409493.2:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.294C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.68C>T
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr87Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

2-74682977-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682977
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682977
    reference: chr 2
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.299C>G
  hgvsp: ENSP00000386937.2:p.Pro100Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.317C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.284C>G
  hgvsp: ENSP00000233331.7:p.Pro95Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.140C>G
  hgvsp: ENSP00000398740.1:p.Pro47Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.284C>G
  hgvsp: ENSP00000387267.1:p.Pro95Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.284C>G
  hgvsp: ENSP00000389887.1:p.Pro95Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.91C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.284C>G
  hgvsp: ENSP00000388677.1:p.Pro95Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.284C>G
  hgvsp: ENSP00000392498.1:p.Pro95Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.429C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.524C>G
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro95Arg
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

2-74682979-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682979
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682979
    reference: chr 2
allele count: 5
allele frequency: 4.119091163725636e-5
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.431C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.286C>T
  hgvsp: ENSP00000233331.7:p.Arg96Cys
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.286C>T
  hgvsp: ENSP00000389887.1:p.Arg96Cys
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.301C>T
  hgvsp: ENSP00000386937.2:p.Arg101Cys
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.319C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.286C>T
  hgvsp: ENSP00000387267.1:p.Arg96Cys
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.286C>T
  hgvsp: ENSP00000388677.1:p.Arg96Cys
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.286C>T
  hgvsp: ENSP00000392498.1:p.Arg96Cys
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.142C>T
  hgvsp: ENSP00000398740.1:p.Arg48Cys
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.526C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.93C>T
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5726
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg96Cys
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

2-74682980-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682980
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682980
    reference: chr 2
allele count: 3
allele frequency: 2.47133254250692e-5
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.287G>A
  hgvsp: ENSP00000387267.1:p.Arg96His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.302G>A
  hgvsp: ENSP00000386937.2:p.Arg101His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.94G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.287G>A
  hgvsp: ENSP00000392498.1:p.Arg96His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.287G>A
  hgvsp: ENSP00000233331.7:p.Arg96His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.287G>A
  hgvsp: ENSP00000389887.1:p.Arg96His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.320G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.143G>A
  hgvsp: ENSP00000398740.1:p.Arg48His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.287G>A
  hgvsp: ENSP00000388677.1:p.Arg96His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.432G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.527G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5726
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg96His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

2-74682986-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682986
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682986
    reference: chr 2
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.293C>T
  hgvsp: ENSP00000392498.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.293C>T
  hgvsp: ENSP00000389887.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.149C>T
  hgvsp: ENSP00000398740.1:p.Pro50Leu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.293C>T
  hgvsp: ENSP00000388677.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.326C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.308C>T
  hgvsp: ENSP00000386937.2:p.Pro103Leu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.293C>T
  hgvsp: ENSP00000387267.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.100C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.293C>T
  hgvsp: ENSP00000233331.7:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.438C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.533C>T
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro98Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

2-74682993-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682993
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682993
    reference: chr 2
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.540C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.300C>T
  hgvsp: ENST00000441673.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.300C>T
  hgvsp: ENST00000431187.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.315C>T
  hgvsp: ENST00000409493.2:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.445C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.300C>T
  hgvsp: ENST00000233331.7:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.107C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.300C>T
  hgvsp: ENST00000452361.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.333C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.300C>T
  hgvsp: ENST00000409917.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.156C>T
  hgvsp: ENST00000455562.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro100Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

2-74682998-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74682998
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74682998
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.305T>C
  hgvsp: ENSP00000387267.1:p.Met102Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.320T>C
  hgvsp: ENSP00000386937.2:p.Met107Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.545T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.112T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.338T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.305T>C
  hgvsp: ENSP00000389887.1:p.Met102Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.305T>C
  hgvsp: ENSP00000233331.7:p.Met102Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.305T>C
  hgvsp: ENSP00000388677.1:p.Met102Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.161T>C
  hgvsp: ENSP00000398740.1:p.Met54Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.305T>C
  hgvsp: ENSP00000392498.1:p.Met102Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.450T>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met102Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

2-74683025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683025
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683025
    reference: chr 2
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.188T>C
  hgvsp: ENSP00000398740.1:p.Met63Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.139T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.572T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.332T>C
  hgvsp: ENSP00000233331.7:p.Met111Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.332T>C
  hgvsp: ENSP00000392498.1:p.Met111Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.365T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.477T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.332T>C
  hgvsp: ENSP00000389887.1:p.Met111Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.347T>C
  hgvsp: ENSP00000386937.2:p.Met116Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.332T>C
  hgvsp: ENSP00000388677.1:p.Met111Thr
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.332T>C
  hgvsp: ENSP00000387267.1:p.Met111Thr
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met111Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP

2-74683030-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683030
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683030
    reference: chr 2
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.337G>A
  hgvsp: ENSP00000392498.1:p.Gly113Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.337G>A
  hgvsp: ENSP00000233331.7:p.Gly113Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.337G>A
  hgvsp: ENSP00000389887.1:p.Gly113Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.337G>A
  hgvsp: ENSP00000388677.1:p.Gly113Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.144G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.352G>A
  hgvsp: ENSP00000386937.2:p.Gly118Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.370G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.337G>A
  hgvsp: ENSP00000387267.1:p.Gly113Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.577G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.193G>A
  hgvsp: ENSP00000398740.1:p.Gly65Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.482G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly113Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

2-74683044-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683044
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683044
    reference: chr 2
allele count: 4
allele frequency: 3.295164346321773e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.496G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.207G>A
  hgvsp: ENST00000455562.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.591G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.384G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.351G>A
  hgvsp: ENST00000452361.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.158G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.351G>A
  hgvsp: ENST00000233331.7:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.351G>A
  hgvsp: ENST00000409917.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.366G>A
  hgvsp: ENST00000409493.2:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.351G>A
  hgvsp: ENST00000431187.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.351G>A
  hgvsp: ENST00000441673.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu117Glu
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

2-74683045-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683045
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683045
    reference: chr 2
allele count: 9
allele frequency: 7.414119779223988e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.352C>G
  hgvsp: ENSP00000389887.1:p.Gln118Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.352C>G
  hgvsp: ENSP00000233331.7:p.Gln118Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.367C>G
  hgvsp: ENSP00000386937.2:p.Gln123Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.352C>G
  hgvsp: ENSP00000387267.1:p.Gln118Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.497C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.592C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.352C>G
  hgvsp: ENSP00000388677.1:p.Gln118Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.159C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.208C>G
  hgvsp: ENSP00000398740.1:p.Gln70Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.352C>G
  hgvsp: ENSP00000392498.1:p.Gln118Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.385C>G
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln118Glu
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

2-74683050-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683050
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683050
    reference: chr 2
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.502C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.372C>T
  hgvsp: ENST00000409493.2:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.357C>T
  hgvsp: ENST00000452361.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.213C>T
  hgvsp: ENST00000455562.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.597C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.357C>T
  hgvsp: ENST00000431187.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.357C>T
  hgvsp: ENST00000409917.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.357C>T
  hgvsp: ENST00000233331.7:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.357C>T
  hgvsp: ENST00000441673.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.390C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.164C>T
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5010
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr119Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

2-74683062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683062
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683062
    reference: chr 2
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.369G>A
  hgvsp: ENST00000233331.7:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.369G>A
  hgvsp: ENST00000441673.1:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.609G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.402G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.369G>A
  hgvsp: ENST00000452361.1:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.369G>A
  hgvsp: ENST00000409917.1:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.369G>A
  hgvsp: ENST00000431187.1:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.176G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.384G>A
  hgvsp: ENST00000409493.2:c.384G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.514G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.225G>A
  hgvsp: ENST00000455562.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.369G>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-74683073-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683073
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683073
    reference: chr 2
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.370+10T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.177+10T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.236T>A
  hgvsp: ENSP00000398740.1:p.Leu79Gln
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.385+10T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.515+10T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.610+10T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.370+10T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.370+10T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.370+10T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.403+10T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.370+10T>A
  variant of: http://identifiers.org/hgnc/13324
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5009
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu79Gln
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

2-74683087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683087
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683087
    reference: chr 2
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.370+24C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.515+24C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.370+24C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.240+10C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.403+24C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.370+24C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.610+24C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.385+24C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.177+24C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.370+24C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.370+24C>T
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5009
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-74683095-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683095
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683095
    reference: chr 2
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.515+32C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.370+32C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.177+32C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.403+32C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.610+32C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.240+18C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.385+32C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.370+32C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.370+32C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.370+32C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.370+32C>G
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5008
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-74683098-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683098
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683098
    reference: chr 2
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.515+35A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.370+35A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.403+35A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.370+35A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.240+21A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.370+35A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.610+35A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.177+35A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.370+35A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.385+35A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.370+35A>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5007
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5728
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

2-74683099-T-TTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683099
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683101
    reference: chr 2
allele count: 2
allele frequency: 1.651145895251304e-5
allele num: 121128
alternate allele: TTA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.610+39_610+40dupTA
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.370+39_370+40dupTA
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.515+39_515+40dupTA
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.370+39_370+40dupTA
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.240+25_240+26dupTA
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.403+39_403+40dupTA
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.370+39_370+40dupTA
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.385+39_385+40dupTA
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.370+39_370+40dupTA
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.177+39_177+40dupTA
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.370+39_370+40dupTA
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5007
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

2-74683103-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683103
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683103
    reference: chr 2
allele count: 2
allele frequency: 1.652974527662529e-5
allele num: 120994
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.177+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.610+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.370+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.370+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.240+26A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.385+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.370+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.370+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.370+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.515+40A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.403+40A>G
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5732
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

2-74683107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683107
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683107
    reference: chr 2
allele count: 1
allele frequency: 8.262414277451872e-6
allele num: 121030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.610+44G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.385+44G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.240+30G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.177+44G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.515+44G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.370+44G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.370+44G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.370+44G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.370+44G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.403+44G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.370+44G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

2-74683180-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683180
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683180
    reference: chr 2
allele count: 1
allele frequency: 8.659508139937652e-6
allele num: 115480
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-95G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-50G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-50G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-50G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-50G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-50G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-50G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-50G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-50G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-50G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-50G>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

2-74683184-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683184
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683184
    reference: chr 2
allele count: 2
allele frequency: 1.740704637237154e-5
allele num: 114896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-46C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-46C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-46C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-46C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-91C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-46C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-46C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-46C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-46C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-46C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-46C>T
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17479
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

2-74683185-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683185
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683185
    reference: chr 2
allele count: 1
allele frequency: 8.707767328456984e-6
allele num: 114840
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-45C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-45C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-45C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-45C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-45C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-45C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-45C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-90C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-45C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-45C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-45C>G
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/2-74683186-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683186
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683186
    reference: chr 2
allele count: 1
allele frequency: 8.705341597604291e-6
allele num: 114872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-44C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-89C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-44C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-44C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-44C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-44C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-44C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-44C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-44C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-44C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-44C>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum

2-74683189-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683189
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683189
    reference: chr 2
allele count: 21
allele frequency: 1.834573854701751e-4
allele num: 114468
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-86T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-41T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-41T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-41T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-41T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-41T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-41T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-41T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-41T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-41T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-41T>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6234
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6672
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17541
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11859
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

2-74683190-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683190
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683190
    reference: chr 2
allele count: 1
allele frequency: 8.739883584750651e-6
allele num: 114418
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-40C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-85C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-40C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-40C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-40C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-40C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-40C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-40C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-40C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-40C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-40C>G
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6767
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2807
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

2-74683197-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683197
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683197
    reference: chr 2
allele count: 1
allele frequency: 8.740953113527499e-6
allele num: 114404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-33A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-33A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-33A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-33A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-33A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-33A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-33A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-33A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-33A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-78A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-33A>G
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

2-74683202-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683202
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683202
    reference: chr 2
allele count: 1
allele frequency: 8.75196919306844e-6
allele num: 114260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-28G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-28G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-28G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-73G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-28G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-28G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-28G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-28G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-28G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-28G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-28G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

2-74683210-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683210
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683210
    reference: chr 2
allele count: 4
allele frequency: 3.504038404260911e-5
allele num: 114154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-20T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-20T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-20T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-20T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-20T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-20T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-20T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-20T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-20T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-65T>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-20T>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-74683214-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683214
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683214
    reference: chr 2
allele count: 2
allele frequency: 1.751773670841727e-5
allele num: 114170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-16C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-16C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-16C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-16C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-16C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-16C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-16C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-16C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-16C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-61C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-16C>T
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8142
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17863
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3266
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/2-74683217-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683217
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683217
    reference: chr 2
allele count: 1
allele frequency: 8.75258201169345e-6
allele num: 114252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-13A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-13A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-13A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-13A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-13A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-13A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-58A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-13A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-13A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-13A>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-13A>C
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/2-74683225-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683225
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683225
    reference: chr 2
allele count: 1
allele frequency: 8.74018913769294e-6
allele num: 114414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-5C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-50C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-5C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-5C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-5C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-5C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-5C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-5C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-5C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-5C>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-5C>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.371-5C>A
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

2-74683226-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683226
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683226
    reference: chr 2
allele count: 1
allele frequency: 8.735455466648032e-6
allele num: 114476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371-4C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386-4C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371-4C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371-4C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516-4C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241-4C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178-4C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404-4C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611-4C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371-4C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-49C>T
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.371-4C>T
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-74683230-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683230
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683230
    reference: chr 2
allele count: 2
allele frequency: 1.743162445308278e-5
allele num: 114734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.178A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.371A>G
  hgvsp: ENSP00000392498.1:p.Asp124Gly
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-45A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.386A>G
  hgvsp: ENSP00000386937.2:p.Asp129Gly
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.611A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.371A>G
  hgvsp: ENSP00000387267.1:p.Asp124Gly
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.371A>G
  hgvsp: ENSP00000233331.7:p.Asp124Gly
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.404A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.516A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.241A>G
  hgvsp: ENSP00000398740.1:p.Met81Val
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.371A>G
  hgvsp: ENSP00000388677.1:p.Asp124Gly
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11853
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp124Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

2-74683242-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683242
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683242
    reference: chr 2
allele count: 5
allele frequency: 4.342464087821994e-5
allele num: 115142
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.383A>G
  hgvsp: ENSP00000392498.1:p.Asn128Ser
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.528A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.623A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.383A>G
  hgvsp: ENSP00000233331.7:p.Asn128Ser
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.398A>G
  hgvsp: ENSP00000386937.2:p.Asn133Ser
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.383A>G
  hgvsp: ENSP00000387267.1:p.Asn128Ser
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.383A>G
  hgvsp: ENSP00000388677.1:p.Asn128Ser
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-33A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.190A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.416A>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.253A>G
  hgvsp: ENSP00000398740.1:p.Ile85Val
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn128Ser
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

2-74683242-ATCTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683242
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683238
    reference: chr 2
allele count: 1
allele frequency: 8.684928175643988e-6
allele num: 115142
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.403_406delTCTC
  hgvsp: ENSP00000386937.2:p.Ser135ProfsTer11
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.388_391delTCTC
  hgvsp: ENSP00000388677.1:p.Ser130ProfsTer11
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.628_631delTCTC
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-28_371-25delTCTC
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.388_391delTCTC
  hgvsp: ENSP00000392498.1:p.Ser130ProfsTer11
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.421_424delTCTC
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.388_391delTCTC
  hgvsp: ENSP00000387267.1:p.Ser130ProfsTer11
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.195_198delTCTC
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.258_261delTCTC
  hgvsp: ENSP00000398740.1:p.Pro88SerfsTer31
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.388_391delTCTC
  hgvsp: ENSP00000233331.7:p.Ser130ProfsTer11
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.533_536delTCTC
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser130ProfsTer11
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: ATCTC
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

2-74683246-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683246
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683246
    reference: chr 2
allele count: 1
allele frequency: 8.675886241779598e-6
allele num: 115262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.257C>T
  hgvsp: ENSP00000398740.1:p.Ser86Phe
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.420C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.402C>T
  hgvsp: ENST00000409493.2:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.627C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.387C>T
  hgvsp: ENST00000441673.1:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.532C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.194C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.387C>T
  hgvsp: ENST00000233331.7:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-29C>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.387C>T
  hgvsp: ENST00000452361.1:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.387C>T
  hgvsp: ENST00000409917.1:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser86Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

2-74683252-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683252
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683252
    reference: chr 2
allele count: 1
allele frequency: 8.637368711995577e-6
allele num: 115776
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.393C>G
  hgvsp: ENST00000233331.7:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.426C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.200C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.393C>G
  hgvsp: ENST00000441673.1:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.408C>G
  hgvsp: ENST00000409493.2:c.408C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.393C>G
  hgvsp: ENST00000452361.1:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.538C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.263C>G
  hgvsp: ENSP00000398740.1:p.Pro88Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.393C>G
  hgvsp: ENST00000409917.1:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.633C>G
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-23C>G
  variant of: http://identifiers.org/hgnc/13324
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro88Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-74683255-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683255
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683255
    reference: chr 2
allele count: 1
allele frequency: 8.616084506556841e-6
allele num: 116062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.396T>A
  hgvsp: ENST00000452361.1:c.396T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.266T>A
  hgvsp: ENSP00000398740.1:p.Leu89His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.541T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.203T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-20T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.396T>A
  hgvsp: ENST00000233331.7:c.396T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.396T>A
  hgvsp: ENST00000409917.1:c.396T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.411T>A
  hgvsp: ENST00000409493.2:c.411T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.396T>A
  hgvsp: ENST00000441673.1:c.396T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.429T>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.636T>A
  variant of: http://identifiers.org/hgnc/13324
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu89His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

2-74683263-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683263
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683263
    reference: chr 2
allele count: 1
allele frequency: 8.547592997811816e-6
allele num: 116992
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.404G>A
  hgvsp: ENSP00000387267.1:p.Arg135Gln
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.644G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.404G>A
  hgvsp: ENSP00000392498.1:p.Arg135Gln
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.404G>A
  hgvsp: ENSP00000233331.7:p.Arg135Gln
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.274G>A
  hgvsp: ENSP00000398740.1:p.Gly92Arg
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.419G>A
  hgvsp: ENSP00000386937.2:p.Arg140Gln
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.404G>A
  hgvsp: ENSP00000388677.1:p.Arg135Gln
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.437G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.549G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.211G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-12G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg135Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

2-74683264-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683264
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683264
    reference: chr 2
allele count: 2
allele frequency: 1.707154685286034e-5
allele num: 117154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.405G>A
  hgvsp: ENST00000409917.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.405G>A
  hgvsp: ENST00000233331.7:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.438G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.405G>A
  hgvsp: ENST00000441673.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.275G>A
  hgvsp: ENSP00000398740.1:p.Gly92Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.420G>A
  hgvsp: ENST00000409493.2:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-11G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.550G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.405G>A
  hgvsp: ENST00000452361.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.645G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.212G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly92Glu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

2-74683264-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683264
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683264
    reference: chr 2
allele count: 2
allele frequency: 1.707154685286034e-5
allele num: 117154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.550G>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.405G>T
  hgvsp: ENST00000233331.7:c.405G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.405G>T
  hgvsp: ENST00000409917.1:c.405G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.405G>T
  hgvsp: ENST00000452361.1:c.405G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.405G>T
  hgvsp: ENST00000441673.1:c.405G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.645G>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.420G>T
  hgvsp: ENST00000409493.2:c.420G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.438G>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-11G>T
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.275G>T
  hgvsp: ENSP00000398740.1:p.Gly92Val
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.212G>T
  variant of: http://identifiers.org/hgnc/13324
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6209
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly92Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

2-74683265-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683265
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683265
    reference: chr 2
allele count: 1
allele frequency: 8.526748409761421e-6
allele num: 117278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.276G>C
  hgvsp: ENST00000455562.1:c.276G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.439G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.421G>C
  hgvsp: ENSP00000386937.2:p.Asp141His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.406G>C
  hgvsp: ENSP00000392498.1:p.Asp136His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.646G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.213G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.406G>C
  hgvsp: ENSP00000388677.1:p.Asp136His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.406G>C
  hgvsp: ENSP00000233331.7:p.Asp136His
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.551G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.371-10G>C
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.406G>C
  hgvsp: ENSP00000387267.1:p.Asp136His
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp136His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

2-74683278-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74683278
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 74683278
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 118582
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000392498
  ensembl transcript: ENST00000441673
  gene symbol: INO80B
  hgvsc: ENST00000441673.1:c.419G>A
  hgvsp: ENSP00000392498.1:p.Gly140Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000386937
  ensembl transcript: ENST00000409493
  gene symbol: INO80B
  hgvsc: ENST00000409493.2:c.434G>A
  hgvsp: ENSP00000386937.2:p.Gly145Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000233331
  ensembl transcript: ENST00000233331
  gene symbol: INO80B
  hgvsc: ENST00000233331.7:c.419G>A
  hgvsp: ENSP00000233331.7:p.Gly140Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000494986
  gene symbol: INO80B
  hgvsc: ENST00000494986.1:n.452G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000473618
  gene symbol: INO80B
  hgvsc: ENST00000473618.1:n.564G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000398740
  ensembl transcript: ENST00000455562
  gene symbol: INO80B
  hgvsc: ENST00000455562.1:c.289G>A
  hgvsp: ENSP00000398740.1:p.Gly97Ser
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000388677
  ensembl transcript: ENST00000452361
  gene symbol: INO80B
  hgvsc: ENST00000452361.1:c.419G>A
  hgvsp: ENSP00000388677.1:p.Gly140Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000387267
  ensembl transcript: ENST00000409917
  gene symbol: INO80B
  hgvsc: ENST00000409917.1:c.419G>A
  hgvsp: ENSP00000387267.1:p.Gly140Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000469849
  gene symbol: INO80B
  hgvsc: ENST00000469849.1:n.226G>A
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115274
  ensembl protein: ENSP00000389887
  ensembl transcript: ENST00000431187
  gene symbol: INO80B
  hgvsc: ENST00000431187.1:c.374G>A
  hgvsp: ENSP00000389887.1:p.Gly125Glu
  variant of: http://identifiers.org/hgnc/13324
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115274
  ensembl transcript: ENST00000471577
  gene symbol: INO80B
  hgvsc: ENST00000471577.1:n.659G>A
  variant of: http://identifiers.org/hgnc/13324
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly140Glu
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 7627
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 692
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2474
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3864
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3588
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27419
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 280
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3523
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3733
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2496
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7859
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.067390570841386e-5
allele num: 65202
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14096
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.251e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

DP
type: SiteQuality
SIO_000300: 2.468416e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3588
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 98
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3930
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3741
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2473
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7934
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2496
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27419
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.167133520074697e-4
allele num: 8568
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: 65202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.467952e6

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.061e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.385e1

FS
type: SiteQuality
SIO_000300: 1.132e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.217e0

GenotypeQuality
all individuals: 111
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3695
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4037
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27420
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 421
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3585
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2498
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7502
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3463
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2473
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537089981247502e-5
allele num: 65058
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13834
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 2.460544e6

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 1.313e1

FS
type: SiteQuality
SIO_000300: 2.848e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.338e0

GenotypeQuality
all individuals: 616
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27421
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4052
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2497
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3585
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2469
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7350
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.75e1
variant carriers: 0

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

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

Latino
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allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

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

ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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DP
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MQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.919e1

QD
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SIO_000300: 1.02e1

GenotypeQuality
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variant carriers: 2

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

European (Non-Finnish)
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allele frequency: 3.079765937788728e-5
allele num: 64940
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.541877389909954e-5
allele num: 64856
num of homozygotes: 0

VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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DP
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MQ
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FS
type: SiteQuality
SIO_000300: 8.8e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.545117428924598e-5
allele num: 64720
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -2.1e-3

VQSLOD
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DP
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ClippingRankSum
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FS
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MQ
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SIO_000300: 6.025e1

BaseQRankSum
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QD
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MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

ReadPosRankSum
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SIO_000300: 1.08e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64602
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African
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South Asian
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allele frequency: 0.0e0
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Latino
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allele num: 11474
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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DP
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MQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 12376
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QD
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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Latino
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South Asian
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East Asian
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European (Non-Finnish)
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allele num: 64582
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European (Finnish)
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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FS
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ClippingRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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European (Non-Finnish)
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Other
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Latino
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allele frequency: 8.716875871687587e-5
allele num: 11472
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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DP
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 143
bin: 4.75e1
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GenotypeQuality
all individuals: 139
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.719916288803627e-5
allele num: 11468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64388
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.54e-1

DP
type: SiteQuality
SIO_000300: 2.440572e6

MQRankSum
type: SiteQuality
SIO_000300: 4.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e0

FS
type: SiteQuality
SIO_000300: 8.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.07e-1

QD
type: SiteQuality
SIO_000300: 1.019e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

GenotypeQuality
all individuals: 651
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2468
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554678026180778e-5
allele num: 64322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11864
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

FS
type: SiteQuality
SIO_000300: 3.184e0

DP
type: SiteQuality
SIO_000300: 2.440385e6

MQ
type: SiteQuality
SIO_000300: 5.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 1.138e1

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.527e0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554678026180778e-5
allele num: 64322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11756
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.440029e6

MQRankSum
type: SiteQuality
SIO_000300: 1.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

FS
type: SiteQuality
SIO_000300: 1.939e0

QD
type: SiteQuality
SIO_000300: 1.094e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2502
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.042535446205171e-4
allele num: 9592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11644
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.44008e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: -1.034e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.251e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

GenotypeQuality
all individuals: 711
bin: 4.75e1
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
all individuals: 46512
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variant carriers: 271

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 393
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 6
allele frequency: 5.772561092938234e-4
allele num: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 30
allele frequency: 1.878051834230625e-3
allele num: 15974
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.209555488358028e-3
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 211
allele frequency: 3.179434633234886e-3
allele num: 66364
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.123207188526007e-3
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.370786516853933e-3
allele num: 890
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.961e0

FS
type: SiteQuality
SIO_000300: 1.114e0

DP
type: SiteQuality
SIO_000300: 3.640437e6

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

VQSLOD
type: SiteQuality
SIO_000300: 4.23e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 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: 10394
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16042
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.012320390396723e-5
allele num: 66394
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.08e-1

FS
type: SiteQuality
SIO_000300: 2.565e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

QD
type: SiteQuality
SIO_000300: 1.292e1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 5.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 3.630518e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1437
bin: 8.25e1
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: 10388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15998
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506477854775535e-5
allele num: 66380
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.01e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.092e1

DP
type: SiteQuality
SIO_000300: 3.631794e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1312
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GenotypeQuality
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GenotypeQuality
all individuals: 255
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GenotypeQuality
all individuals: 1765
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16052
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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: 0.0e0
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ClippingRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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SIO_000300: 6.3e-3

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.504528631179851e-5
allele num: 66466
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

East Asian
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allele frequency: 3.467406380027739e-4
allele num: 8652
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

East Asian
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allele frequency: 0.0e0
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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: 0.0e0
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DP
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MQRankSum
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

Other
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num of homozygotes: 0

East Asian
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allele frequency: 3.466605038132656e-4
allele num: 8654
num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.499925003749813e-5
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num of homozygotes: 0

European (Finnish)
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Latino
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num of homozygotes: 0

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

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

Latino
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num of homozygotes: 0

African
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East Asian
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European (Non-Finnish)
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num of homozygotes: 0

South Asian
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Other
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European (Finnish)
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MQ
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FS
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ClippingRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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DP
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FS
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QD
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MQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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Latino
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East Asian
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InbreedingCoeff
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FS
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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MQ
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QD
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ClippingRankSum
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SIO_000300: 9.6e-1

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

Latino
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allele num: 11578
num of homozygotes: 0

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

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

South Asian
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Other
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African
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European (Finnish)
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East Asian
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Latino
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BaseQRankSum
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SIO_000300: -2.319e0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

African
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 5.993586862057598e-5
allele num: 66738
num of homozygotes: 0

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

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

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

Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.34855704396296e-4
allele num: 66738
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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QD
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

Latino
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South Asian
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African
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European (Finnish)
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East Asian
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Other
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BaseQRankSum
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MQ
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ClippingRankSum
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DP
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FS
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QD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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

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

Latino
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South Asian
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African
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Other
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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European (Finnish)
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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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DP
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MQ
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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

QD
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SIO_000300: 9.800000000000001e0

InbreedingCoeff
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SIO_000300: 1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.28e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

DP
type: SiteQuality
SIO_000300: 3.648364e6

FS
type: SiteQuality
SIO_000300: 1.319e0

VQSLOD
type: SiteQuality
SIO_000300: -1.18e0

MQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

South Asian
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allele frequency: 1.212709192335678e-4
allele num: 16492
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.091e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e-1

MQRankSum
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SIO_000300: 8.49e-1

ReadPosRankSum
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SIO_000300: -8.52e-1

BaseQRankSum
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QD
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SIO_000300: 1.618e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

DP
type: SiteQuality
SIO_000300: 3.647606e6

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.002552169343942e-5
allele num: 66610
num of homozygotes: 0

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

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

African
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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
allele num: 16478
num of homozygotes: 0

MQRankSum
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SIO_000300: 6.65e-1

FS
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SIO_000300: 7.129e0

VQSLOD
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InbreedingCoeff
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SIO_000300: 1.1e-3

ClippingRankSum
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SIO_000300: 3.68e0

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: -1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

DP
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SIO_000300: 3.644259e6

QD
type: SiteQuality
SIO_000300: 6.96e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

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

Latino
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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: 8652
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.059e0

VQSLOD
type: SiteQuality
SIO_000300: -1.84e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

BaseQRankSum
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SIO_000300: -3.883e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.01e-1

QD
type: SiteQuality
SIO_000300: 1.087e1

DP
type: SiteQuality
SIO_000300: 3.642295e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535673700052213e-5
allele num: 65118
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0819e1

MQRankSum
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SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 1.271e1

InbreedingCoeff
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SIO_000300: 2.0e-4

VQSLOD
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 7.62e-1

BaseQRankSum
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SIO_000300: 1.24e0

DP
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SIO_000300: 1.913976e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.079955648638659e-5
allele num: 64936
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12356
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.146e-1

QD
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ClippingRankSum
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SIO_000300: 4.51e-1

MQRankSum
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BaseQRankSum
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MQ
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DP
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InbreedingCoeff
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FS
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ReadPosRankSum
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SIO_000300: -6.31e-1

GenotypeQuality
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variant carriers: 1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

East Asian
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allele frequency: 1.164958061509786e-4
allele num: 8584
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64914
num of homozygotes: 0

South Asian
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VQSLOD
type: SiteQuality
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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DP
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ReadPosRankSum
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FS
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele num: 8584
num of homozygotes: 0

Other
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allele num: 844
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 12300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64946
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.86e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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QD
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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MQ
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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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8538
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 703
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19755
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4276
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1429
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3267
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.233425840271354e-4
allele num: 64860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10112
num of homozygotes: 0

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

Latino
type: Population
allele count: 13
allele frequency: 1.132798884628791e-3
allele num: 11476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12004
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e0

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

DP
type: SiteQuality
SIO_000300: 1.907239e6

QD
type: SiteQuality
SIO_000300: 1.516e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

GenotypeQuality
all individuals: 847
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7782
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4271
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3107
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20281
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8518
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 874
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.54206760424377e-5
allele num: 64848
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.33e-1

DP
type: SiteQuality
SIO_000300: 1.907354e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.226e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

GenotypeQuality
all individuals: 390
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4230
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3097
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8509
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3091
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22257
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7814
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11934
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541782300339192e-5
allele num: 64860
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 3.901e0

MQ
type: SiteQuality
SIO_000300: 5.844e1

QD
type: SiteQuality
SIO_000300: 1.486e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.17e0

DP
type: SiteQuality
SIO_000300: 1.910032e6

VQSLOD
type: SiteQuality
SIO_000300: -2.501e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.926e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e0

GenotypeQuality
all individuals: 22542
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3089
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1423
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7778
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3021
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3256
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4217
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8504
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 369
bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11824
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542781326174828e-5
allele num: 64818
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.34e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

VQSLOD
type: SiteQuality
SIO_000300: 4.58e-1

FS
type: SiteQuality
SIO_000300: 2.746e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.35e-1

DP
type: SiteQuality
SIO_000300: 1.91145e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 205
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4209
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2818
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7795
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23006
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3100
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8509
bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64808
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 3.41705108491372e-4
allele num: 11706
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

FS
type: SiteQuality
SIO_000300: 7.08e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.305e1

VQSLOD
type: SiteQuality
SIO_000300: 9.429999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 1.913472e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.309e0

GenotypeQuality
all individuals: 358
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3069
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3087
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4210
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7792
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8505
bin: 9.75e1
variant carriers: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64808
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11702
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.328830926874709e-4
allele num: 8588
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.32e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

FS
type: SiteQuality
SIO_000300: 6.474e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.139e0

MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: -5.555e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.916697e6

GenotypeQuality
all individuals: 325
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4219
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3083
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3114
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8502
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23870
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3272
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7822
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542448173741362e-5
allele num: 64832
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.146e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 1.918675e6

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
SIO_000300: 3.95e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.65e0

QD
type: SiteQuality
SIO_000300: 1.427e1

GenotypeDepth
all individuals: 3570
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 774
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24232
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1420
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3169
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4221
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3076
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8502
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11820
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.515610791148833e-4
allele num: 6598
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -3.727e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
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DP
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SIO_000300: 1.923328e6

VQSLOD
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: 1.02e0

MQ
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SIO_000300: 5.962e1

MQRankSum
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SIO_000300: -1.141e0

QD
type: SiteQuality
SIO_000300: 1.064e1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 8.428860418071477e-5
allele num: 11864
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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QD
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MQ
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DP
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.079671091127467e-5
allele num: 64942
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.926192e6

ClippingRankSum
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SIO_000300: -1.128e0

FS
type: SiteQuality
SIO_000300: 8.611000000000001e0

InbreedingCoeff
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SIO_000300: 4.7e-3

VQSLOD
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SIO_000300: 8.0e-1

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 2.46e0

MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

QD
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SIO_000300: 1.193e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65032
num of homozygotes: 0

South Asian
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allele count: 5
allele frequency: 4.078968836678088e-4
allele num: 12258
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 1.933034e6

MQRankSum
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MQ
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InbreedingCoeff
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SIO_000300: 1.8e-3

FS
type: SiteQuality
SIO_000300: 4.399e0

BaseQRankSum
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SIO_000300: 2.36e0

QD
type: SiteQuality
SIO_000300: 1.28e1

VQSLOD
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SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele frequency: 1.537704514700455e-5
allele num: 65032
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11506
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South Asian
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allele count: 0
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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QD
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele num: 10288
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Latino
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East Asian
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MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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MQ
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InbreedingCoeff
type: SiteQuality
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8495
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variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65262
num of homozygotes: 0

South Asian
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East Asian
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African
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Latino
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Other
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European (Finnish)
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.85e0

DP
type: SiteQuality
SIO_000300: 1.945065e6

QD
type: SiteQuality
SIO_000300: 1.142e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

GenotypeDepth
all individuals: 175
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2434
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3101
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 279
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4253
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3280
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8494
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 468
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25741
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7985
bin: 6.75e1
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
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527603800678256e-5
allele num: 65462
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.51e1

VQSLOD
type: SiteQuality
SIO_000300: -7.547e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

DP
type: SiteQuality
SIO_000300: 1.956374e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 1.0882e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

GenotypeDepth
all individuals: 244
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variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
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GenotypeQuality
all individuals: 272
bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3277
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25705
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
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: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053062221408072e-5
allele num: 65508
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.76e-1

FS
type: SiteQuality
SIO_000300: 5.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.452e1

VQSLOD
type: SiteQuality
SIO_000300: 4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.44e-1

DP
type: SiteQuality
SIO_000300: 1.95713e6

GenotypeDepth
all individuals: 163
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variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
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variant carriers: 0

GenotypeQuality
all individuals: 8497
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 7997
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variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3101
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
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variant carriers: 0

GenotypeQuality
all individuals: 2375
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
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variant carriers: 0

GenotypeQuality
all individuals: 25705
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4260
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3277
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13662
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65508
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.157407407407407e-3
allele num: 864
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 1.452e1

DP
type: SiteQuality
SIO_000300: 1.95713e6

FS
type: SiteQuality
SIO_000300: 5.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.44e-1

GenotypeDepth
all individuals: 812
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variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 137
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variant carriers: 0

GenotypeQuality
all individuals: 462
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variant carriers: 0

GenotypeQuality
all individuals: 25894
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 1998
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variant carriers: 0

GenotypeQuality
all individuals: 2328
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variant carriers: 0

GenotypeQuality
all individuals: 3108
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variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 130
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variant carriers: 0

GenotypeQuality
all individuals: 424
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GenotypeQuality
all individuals: 1427
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 114
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variant carriers: 0

GenotypeQuality
all individuals: 265
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variant carriers: 0

GenotypeQuality
all individuals: 8496
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8015
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 3272
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65536
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: 868
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13744
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

FS
type: SiteQuality
SIO_000300: 1.456e0

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 1.548e1

DP
type: SiteQuality
SIO_000300: 1.9586e6

VQSLOD
type: SiteQuality
SIO_000300: 2.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

GenotypeDepth
all individuals: 19081
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 1601
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3276
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variant carriers: 0

GenotypeQuality
all individuals: 8111
bin: 6.75e1
variant carriers: 0