16-30012143-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012143
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012143
    reference: chr 16
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.270A>G
  hgvsp: ENST00000567987.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.270A>G
  hgvsp: ENST00000563197.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.270A>G
  hgvsp: ENST00000304516.7:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.270A>G
  hgvsp: ENST00000562441.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.270A>G
  hgvsp: ENST00000567065.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.307A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.270A>G
  hgvsp: ENST00000567254.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.343A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.270A>G
  hgvsp: ENST00000567705.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8627
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40612
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr90Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP

16-30012145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012145
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012145
    reference: chr 16
allele count: 9
allele frequency: 7.433102081268583e-5
allele num: 121080
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.272C>T
  hgvsp: ENSP00000457016.1:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.272C>T
  hgvsp: ENSP00000454924.1:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.272C>T
  hgvsp: ENSP00000303977.7:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.309C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.345C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.272C>T
  hgvsp: ENSP00000461808.1:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.272C>T
  hgvsp: ENSP00000456073.1:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.272C>T
  hgvsp: ENSP00000454665.1:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.272C>T
  hgvsp: ENSP00000459432.1:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23680
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro91Leu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

16-30012146-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012146
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012146
    reference: chr 16
allele count: 93
allele frequency: 7.680364693446089e-4
allele num: 121088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.346G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.273G>A
  hgvsp: ENST00000304516.7:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.310G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.273G>A
  hgvsp: ENST00000562441.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.273G>A
  hgvsp: ENST00000567065.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.273G>A
  hgvsp: ENST00000567254.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.273G>A
  hgvsp: ENST00000567705.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.273G>A
  hgvsp: ENST00000563197.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.273G>A
  hgvsp: ENST00000567987.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 23789
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8435
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 23694
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro91Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

16-30012148-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012148
    reference: chr 16
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.275C>G
  hgvsp: ENSP00000461808.1:p.Ala92Gly
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.275C>G
  hgvsp: ENSP00000454924.1:p.Ala92Gly
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.348C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.275C>G
  hgvsp: ENSP00000459432.1:p.Ala92Gly
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.275C>G
  hgvsp: ENSP00000303977.7:p.Ala92Gly
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.275C>G
  hgvsp: ENSP00000456073.1:p.Ala92Gly
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.275C>G
  hgvsp: ENSP00000457016.1:p.Ala92Gly
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.275C>G
  hgvsp: ENSP00000454665.1:p.Ala92Gly
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.312C>G
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala92Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

16-30012148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012148
    reference: chr 16
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.275C>T
  hgvsp: ENSP00000457016.1:p.Ala92Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.275C>T
  hgvsp: ENSP00000459432.1:p.Ala92Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.275C>T
  hgvsp: ENSP00000454665.1:p.Ala92Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.348C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.275C>T
  hgvsp: ENSP00000454924.1:p.Ala92Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.275C>T
  hgvsp: ENSP00000456073.1:p.Ala92Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.312C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.275C>T
  hgvsp: ENSP00000303977.7:p.Ala92Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.275C>T
  hgvsp: ENSP00000461808.1:p.Ala92Val
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala92Val
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-30012153-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012153
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012153
    reference: chr 16
allele count: 12
allele frequency: 9.912112601599155e-5
allele num: 121064
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.280A>G
  hgvsp: ENSP00000454665.1:p.Lys94Glu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.280A>G
  hgvsp: ENSP00000303977.7:p.Lys94Glu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.353A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.280A>G
  hgvsp: ENSP00000459432.1:p.Lys94Glu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.280A>G
  hgvsp: ENSP00000461808.1:p.Lys94Glu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.280A>G
  hgvsp: ENSP00000456073.1:p.Lys94Glu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.280A>G
  hgvsp: ENSP00000454924.1:p.Lys94Glu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.317A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.280A>G
  hgvsp: ENSP00000457016.1:p.Lys94Glu
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys94Glu
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

16-30012154-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012154
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012154
    reference: chr 16
allele count: 1
allele frequency: 8.259957378619926e-6
allele num: 121066
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.281A>G
  hgvsp: ENSP00000459432.1:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.281A>G
  hgvsp: ENSP00000456073.1:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.354A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.281A>G
  hgvsp: ENSP00000457016.1:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.281A>G
  hgvsp: ENSP00000454665.1:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.281A>G
  hgvsp: ENSP00000454924.1:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.281A>G
  hgvsp: ENSP00000303977.7:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.318A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.281A>G
  hgvsp: ENSP00000461808.1:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1866
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys94Arg
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

16-30012157-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012157
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012157
    reference: chr 16
allele count: 2
allele frequency: 1.65218253312626e-5
allele num: 121052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.321G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.284G>A
  hgvsp: ENSP00000454665.1:p.Arg95Lys
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.357G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.284G>A
  hgvsp: ENSP00000456073.1:p.Arg95Lys
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.284G>A
  hgvsp: ENSP00000303977.7:p.Arg95Lys
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.284G>A
  hgvsp: ENSP00000459432.1:p.Arg95Lys
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.284G>A
  hgvsp: ENSP00000457016.1:p.Arg95Lys
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.284G>A
  hgvsp: ENSP00000461808.1:p.Arg95Lys
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.284G>A
  hgvsp: ENSP00000454924.1:p.Arg95Lys
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg95Lys
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

16-30012160-GAGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012160
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012157
    reference: chr 16
allele count: 207
allele frequency: 1.710319755432537e-3
allele num: 121030
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.284+10_284+12delAGA
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.284+10_284+12delAGA
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.284+10_284+12delAGA
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.284+10_284+12delAGA
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.284+10_284+12delAGA
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.284+10_284+12delAGA
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.357+10_357+12delAGA
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.284+10_284+12delAGA
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.321+10_321+12delAGA
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23400
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23811
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 3.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8419
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40452
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: c.284+10_284+12delAGA
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: GAGA
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-30012173-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012173
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012173
    reference: chr 16
allele count: 2
allele frequency: 1.655053706492776e-5
allele num: 120842
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.284+16A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.284+16A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.284+16A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.284+16A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.357+16A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.284+16A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.284+16A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.284+16A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.321+16A>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8445
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1870
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 39561
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

16-30012176-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012176
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012176
    reference: chr 16
allele count: 2
allele frequency: 1.656369569178275e-5
allele num: 120746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.284+19C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.284+19C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.284+19C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.321+19C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.284+19C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.357+19C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.284+19C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.284+19C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.284+19C>G
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8427
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

16-30012182-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012182
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012182
    reference: chr 16
allele count: 5
allele frequency: 4.149102134298138e-5
allele num: 120508
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.321+25G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.284+25G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.284+25G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.284+25G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.357+25G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.284+25G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.284+25G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.284+25G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.284+25G>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8368
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23715
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8312
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38473
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-30012192-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012192
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012192
    reference: chr 16
allele count: 1
allele frequency: 8.321544478655239e-6
allele num: 120170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.284+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.284+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.357+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.284+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.284+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.284+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.284+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.321+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.284+35G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21950
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

16-30012202-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012202
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012202
    reference: chr 16
allele count: 27
allele frequency: 2.255337632396672e-4
allele num: 119716
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.284+45G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.284+45G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.284+45G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.357+45G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.284+45G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.284+45G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.284+45G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.284+45G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.321+45G>C
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8011
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21693
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2552
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

16-30012203-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012203
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012203
    reference: chr 16
allele count: 1
allele frequency: 8.364980844193866e-6
allele num: 119546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.284+46C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.284+46C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.284+46C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.284+46C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.284+46C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.357+46C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.284+46C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.321+46C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.284+46C>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8057
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

16-30012204-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012204
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012204
    reference: chr 16
allele count: 2
allele frequency: 1.672996168838773e-5
allele num: 119546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-46G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23380
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37943
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

16-30012207-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012207
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012207
    reference: chr 16
allele count: 1
allele frequency: 8.379139294811638e-6
allele num: 119344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-43T>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-43T>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-43T>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-43T>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-43T>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-43T>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-43T>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-43T>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-43T>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7977
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

16-30012211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012211
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012211
    reference: chr 16
allele count: 1
allele frequency: 8.389965601141035e-6
allele num: 119190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-39C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-39C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-39C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-39C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-39C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-39C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-39C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-39C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-39C>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2631
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

16-30012217-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012217
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012217
    reference: chr 16
allele count: 2
allele frequency: 1.681718043152885e-5
allele num: 118926
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-33G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-33G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-33G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-33G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-33G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-33G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-33G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-33G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-33G>C
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23594
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38394
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8062
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

16-30012226-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012226
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012226
    reference: chr 16
allele count: 1
allele frequency: 8.467400508044031e-6
allele num: 118100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-24G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-24G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-24G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-24G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-24G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-24G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-24G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-24G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-24G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7943
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

16-30012228-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012228
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012228
    reference: chr 16
allele count: 1
allele frequency: 8.480901010923401e-6
allele num: 117912
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-22C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-22C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-22C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-22C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-22C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-22C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-22C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-22C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-22C>G
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2926
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS

http://identifiers.org/exac.variant/16-30012229-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012229
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012229
    reference: chr 16
allele count: 1
allele frequency: 8.487811502682149e-6
allele num: 117816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-21C>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-21C>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-21C>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-21C>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-21C>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-21C>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-21C>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-21C>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-21C>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1804
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37535
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

16-30012231-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012231
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012231
    reference: chr 16
allele count: 1
allele frequency: 8.486370888353305e-6
allele num: 117836
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-19C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-19C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-19C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-19C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-19C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-19C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-19C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-19C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-19C>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21015
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3120
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37808
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

16-30012232-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012232
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012232
    reference: chr 16
allele count: 1
allele frequency: 8.491559389966374e-6
allele num: 117764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-18G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-18G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-18G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-18G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-18G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-18G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-18G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-18G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-18G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37881
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-30012232-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012232
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012232
    reference: chr 16
allele count: 2
allele frequency: 1.698311877993275e-5
allele num: 117764
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-18G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-18G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-18G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-18G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-18G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-18G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-18G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-18G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-18G>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3158
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

16-30012234-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012234
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012234
    reference: chr 16
allele count: 4
allele frequency: 3.401591945030274e-5
allele num: 117592
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-16C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-16C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-16C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-16C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-16C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-16C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-16C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-16C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-16C>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1809
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2495
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

16-30012247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012247
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012247
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 116506
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.285-3C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.285-3C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.285-3C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.285-3C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.285-3C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.285-3C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.285-3C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.322-3C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.358-3C>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7814
  bin: 6.75e1
  variant carriers: 0
hgvs: c.285-3C>T
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

16-30012264-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012264
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012264
    reference: chr 16
allele count: 130
allele frequency: 1.143681599042827e-3
allele num: 113668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.299C>T
  hgvsp: ENSP00000461808.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.299C>T
  hgvsp: ENSP00000457016.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.336C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.299C>T
  hgvsp: ENSP00000459432.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.299C>T
  hgvsp: ENSP00000303977.7:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.299C>T
  hgvsp: ENSP00000454665.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.299C>T
  hgvsp: ENSP00000456073.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.299C>T
  hgvsp: ENSP00000454924.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.372C>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7736
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19934
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22156
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro100Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

16-30012265-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012265
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012265
    reference: chr 16
allele count: 4
allele frequency: 3.518834561993068e-5
allele num: 113674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.300G>A
  hgvsp: ENST00000304516.7:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.300G>A
  hgvsp: ENST00000562441.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.300G>A
  hgvsp: ENST00000567705.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.300G>A
  hgvsp: ENST00000567254.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.373G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.300G>A
  hgvsp: ENST00000567065.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.300G>A
  hgvsp: ENST00000563197.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.300G>A
  hgvsp: ENST00000567987.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.337G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2553
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro100Pro
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

16-30012265-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012265
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012265
    reference: chr 16
allele count: 2
allele frequency: 1.759417280996534e-5
allele num: 113674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.300G>C
  hgvsp: ENST00000567987.1:c.300G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.300G>C
  hgvsp: ENST00000567065.1:c.300G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.300G>C
  hgvsp: ENST00000567254.1:c.300G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.300G>C
  hgvsp: ENST00000304516.7:c.300G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.300G>C
  hgvsp: ENST00000562441.1:c.300G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.300G>C
  hgvsp: ENST00000567705.1:c.300G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.337G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.300G>C
  hgvsp: ENST00000563197.1:c.300G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.373G>C
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35739
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7651
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro100Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

16-30012265-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012265
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012265
    reference: chr 16
allele count: 1
allele frequency: 8.79708640498267e-6
allele num: 113674
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.300G>T
  hgvsp: ENST00000304516.7:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.300G>T
  hgvsp: ENST00000562441.1:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.300G>T
  hgvsp: ENST00000563197.1:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.300G>T
  hgvsp: ENST00000567254.1:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.300G>T
  hgvsp: ENST00000567065.1:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.337G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.373G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.300G>T
  hgvsp: ENST00000567987.1:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.300G>T
  hgvsp: ENST00000567705.1:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro100Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-30012274-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012274
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012274
    reference: chr 16
allele count: 2
allele frequency: 1.773521326593952e-5
allele num: 112770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.309C>T
  hgvsp: ENST00000304516.7:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.309C>T
  hgvsp: ENST00000563197.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.309C>T
  hgvsp: ENST00000562441.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.382C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.309C>T
  hgvsp: ENST00000567254.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.309C>T
  hgvsp: ENST00000567705.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.346C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.309C>T
  hgvsp: ENST00000567987.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.309C>T
  hgvsp: ENST00000567065.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19963
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly103Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

16-30012275-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012275
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012275
    reference: chr 16
allele count: 26
allele frequency: 2.309961263726501e-4
allele num: 112556
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.310G>A
  hgvsp: ENSP00000459432.1:p.Ala104Thr
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.310G>A
  hgvsp: ENSP00000303977.7:p.Ala104Thr
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.310G>A
  hgvsp: ENSP00000454924.1:p.Ala104Thr
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.310G>A
  hgvsp: ENSP00000461808.1:p.Ala104Thr
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.310G>A
  hgvsp: ENSP00000456073.1:p.Ala104Thr
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.310G>A
  hgvsp: ENSP00000457016.1:p.Ala104Thr
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.310G>A
  hgvsp: ENSP00000454665.1:p.Ala104Thr
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.383G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.347G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35694
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala104Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

16-30012275-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012275
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012275
    reference: chr 16
allele count: 80
allele frequency: 7.107573119158464e-4
allele num: 112556
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.310G>T
  hgvsp: ENSP00000454924.1:p.Ala104Ser
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.347G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.383G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.310G>T
  hgvsp: ENSP00000461808.1:p.Ala104Ser
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.310G>T
  hgvsp: ENSP00000456073.1:p.Ala104Ser
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.310G>T
  hgvsp: ENSP00000454665.1:p.Ala104Ser
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.310G>T
  hgvsp: ENSP00000303977.7:p.Ala104Ser
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.310G>T
  hgvsp: ENSP00000457016.1:p.Ala104Ser
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.310G>T
  hgvsp: ENSP00000459432.1:p.Ala104Ser
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22127
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 19937
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35694
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala104Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

16-30012276-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012276
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012276
    reference: chr 16
allele count: 1
allele frequency: 8.878471482349599e-6
allele num: 112632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.311C>T
  hgvsp: ENSP00000454924.1:p.Ala104Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.348C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.384C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.311C>T
  hgvsp: ENSP00000461808.1:p.Ala104Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.311C>T
  hgvsp: ENSP00000456073.1:p.Ala104Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.311C>T
  hgvsp: ENSP00000303977.7:p.Ala104Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.311C>T
  hgvsp: ENSP00000454665.1:p.Ala104Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.311C>T
  hgvsp: ENSP00000457016.1:p.Ala104Val
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.311C>T
  hgvsp: ENSP00000459432.1:p.Ala104Val
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2470
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala104Val
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

16-30012277-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012277
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012277
    reference: chr 16
allele count: 1
allele frequency: 8.874846908890822e-6
allele num: 112678
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.312C>G
  hgvsp: ENST00000563197.1:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.312C>G
  hgvsp: ENST00000567987.1:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.312C>G
  hgvsp: ENST00000567065.1:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.312C>G
  hgvsp: ENST00000562441.1:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.312C>G
  hgvsp: ENST00000567254.1:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.312C>G
  hgvsp: ENST00000567705.1:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.312C>G
  hgvsp: ENST00000304516.7:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.349C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.385C>G
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3859
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35923
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala104Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

16-30012287-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012287
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012287
    reference: chr 16
allele count: 11
allele frequency: 9.958175662218681e-5
allele num: 110462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.322T>C
  hgvsp: ENSP00000459432.1:p.Ser108Pro
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.322T>C
  hgvsp: ENSP00000457016.1:p.Ser108Pro
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.322T>C
  hgvsp: ENSP00000454924.1:p.Ser108Pro
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.322T>C
  hgvsp: ENSP00000303977.7:p.Ser108Pro
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.322T>C
  hgvsp: ENSP00000454665.1:p.Ser108Pro
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.322T>C
  hgvsp: ENSP00000456073.1:p.Ser108Pro
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.322T>C
  hgvsp: ENSP00000461808.1:p.Ser108Pro
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.395T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.359T>C
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22177
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.75e1
  variant carriers: 1
hgvs: p.Ser108Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

16-30012299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012299
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012299
    reference: chr 16
allele count: 1
allele frequency: 8.993291004910338e-6
allele num: 111194
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.334C>T
  hgvsp: ENST00000563197.1:c.334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.371C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.8C>T
  hgvsp: ENST00000562291.2:c.8C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.407C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.334C>T
  hgvsp: ENST00000567065.1:c.334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.334C>T
  hgvsp: ENST00000567254.1:c.334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.334C>T
  hgvsp: ENST00000304516.7:c.334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.334C>T
  hgvsp: ENST00000562441.1:c.334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.334C>T
  hgvsp: ENST00000567987.1:c.334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.334C>T
  hgvsp: ENST00000567705.1:c.334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu112Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

16-30012311-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012311
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012311
    reference: chr 16
allele count: 1
allele frequency: 9.020386072523904e-6
allele num: 110860
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.346A>G
  hgvsp: ENSP00000457016.1:p.Thr116Ala
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.346A>G
  hgvsp: ENSP00000459432.1:p.Thr116Ala
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.419A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.346A>G
  hgvsp: ENSP00000454924.1:p.Thr116Ala
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.346A>G
  hgvsp: ENSP00000454665.1:p.Thr116Ala
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.346A>G
  hgvsp: ENSP00000456073.1:p.Thr116Ala
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.383A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.346A>G
  hgvsp: ENSP00000461808.1:p.Thr116Ala
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.20A>G
  hgvsp: ENSP00000458392.1:p.Thr8Ala
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.346A>G
  hgvsp: ENSP00000303977.7:p.Thr116Ala
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr116Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-30012322-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012322
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012322
    reference: chr 16
allele count: 1
allele frequency: 9.049446173894157e-6
allele num: 110504
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.357C>G
  hgvsp: ENST00000567987.1:c.357C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.357C>G
  hgvsp: ENST00000567705.1:c.357C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.31C>G
  hgvsp: ENST00000562291.2:c.31C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.357C>G
  hgvsp: ENST00000567065.1:c.357C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.357C>G
  hgvsp: ENST00000567254.1:c.357C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.357C>G
  hgvsp: ENST00000562441.1:c.357C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.394C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.357C>G
  hgvsp: ENST00000563197.1:c.357C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.430C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.357C>G
  hgvsp: ENST00000304516.7:c.357C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro119Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-30012322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012322
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012322
    reference: chr 16
allele count: 7
allele frequency: 6.334612321725911e-5
allele num: 110504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.357C>T
  hgvsp: ENST00000567987.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.31C>T
  hgvsp: ENST00000562291.2:c.31C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.357C>T
  hgvsp: ENST00000567705.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.357C>T
  hgvsp: ENST00000562441.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.357C>T
  hgvsp: ENST00000304516.7:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.394C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.357C>T
  hgvsp: ENST00000567065.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.357C>T
  hgvsp: ENST00000567254.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.430C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.357C>T
  hgvsp: ENST00000563197.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro119Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

16-30012323-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012323
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012323
    reference: chr 16
allele count: 201
allele frequency: 1.819399688620153e-3
allele num: 110476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.358C>T
  hgvsp: ENSP00000454924.1:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.358C>T
  hgvsp: ENSP00000457016.1:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.395C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.431C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.358C>T
  hgvsp: ENSP00000303977.7:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.32C>T
  hgvsp: ENSP00000458392.1:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.358C>T
  hgvsp: ENSP00000456073.1:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.358C>T
  hgvsp: ENSP00000459432.1:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.358C>T
  hgvsp: ENSP00000454665.1:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.358C>T
  hgvsp: ENSP00000461808.1:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22517
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7722
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 19823
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu120Phe
num of homozygotes: 2
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

16-30012334-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012334
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012334
    reference: chr 16
allele count: 3
allele frequency: 2.722570106180234e-5
allele num: 110190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.369C>T
  hgvsp: ENST00000567254.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.369C>T
  hgvsp: ENST00000563197.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.43C>T
  hgvsp: ENST00000562291.2:c.43C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.369C>T
  hgvsp: ENST00000567065.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.369C>T
  hgvsp: ENST00000567987.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.442C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.369C>T
  hgvsp: ENST00000304516.7:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.369C>T
  hgvsp: ENST00000562441.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.369C>T
  hgvsp: ENST00000567705.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.406C>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3913
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser123Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

16-30012335-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012335
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012335
    reference: chr 16
allele count: 144
allele frequency: 1.307142079082096e-3
allele num: 110164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.370G>A
  hgvsp: ENSP00000459432.1:p.Gly124Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.370G>A
  hgvsp: ENSP00000457016.1:p.Gly124Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.443G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.44G>A
  hgvsp: ENSP00000458392.1:p.Gly16Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.370G>A
  hgvsp: ENSP00000456073.1:p.Gly124Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.370G>A
  hgvsp: ENSP00000454924.1:p.Gly124Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.407G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.370G>A
  hgvsp: ENSP00000461808.1:p.Gly124Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.370G>A
  hgvsp: ENSP00000454665.1:p.Gly124Arg
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.370G>A
  hgvsp: ENSP00000303977.7:p.Gly124Arg
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19722
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly124Arg
num of homozygotes: 1
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

16-30012340-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012340
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012340
    reference: chr 16
allele count: 1
allele frequency: 9.083312138938343e-6
allele num: 110092
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.375C>G
  hgvsp: ENST00000567065.1:c.375C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.448C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.375C>G
  hgvsp: ENST00000563197.1:c.375C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.375C>G
  hgvsp: ENST00000567987.1:c.375C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.412C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.375C>G
  hgvsp: ENST00000304516.7:c.375C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.49C>G
  hgvsp: ENST00000562291.2:c.49C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.375C>G
  hgvsp: ENST00000562441.1:c.375C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.375C>G
  hgvsp: ENST00000567254.1:c.375C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.375C>G
  hgvsp: ENST00000567705.1:c.375C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1449
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val125Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum

16-30012360-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012360
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012360
    reference: chr 16
allele count: 2
allele frequency: 1.826083780723859e-5
allele num: 109524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.69C>T
  hgvsp: ENSP00000458392.1:p.Ser24Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.395C>T
  hgvsp: ENSP00000454665.1:p.Ser132Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.395C>T
  hgvsp: ENSP00000303977.7:p.Ser132Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.395C>T
  hgvsp: ENSP00000457016.1:p.Ser132Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.432C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.395C>T
  hgvsp: ENSP00000456073.1:p.Ser132Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.395C>T
  hgvsp: ENSP00000459432.1:p.Ser132Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.395C>T
  hgvsp: ENSP00000461808.1:p.Ser132Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.395C>T
  hgvsp: ENSP00000454924.1:p.Ser132Leu
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.468C>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser132Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

16-30012368-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012368
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012368
    reference: chr 16
allele count: 1
allele frequency: 9.155496960375008e-6
allele num: 109224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+7T>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+7T>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+7T>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.469+7T>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.396+7T>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.396+7T>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+7T>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.433+7T>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+7T>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+7T>G
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.396+7T>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

16-30012372-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012372
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012372
    reference: chr 16
allele count: 14
allele frequency: 1.284922353977752e-4
allele num: 108956
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.469+11G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.433+11G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+11G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.396+11G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+11G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+11G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+11G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+11G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.396+11G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+11G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21706
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4917
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS

16-30012377-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012377
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012377
    reference: chr 16
allele count: 4
allele frequency: 3.680191369951237e-5
allele num: 108690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.469+16G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+16G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+16G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.433+16G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+16G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+16G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.396+16G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+16G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+16G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.396+16G>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7506
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21384
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 3.25e1
  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: G
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

16-30012379-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012379
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012380
    reference: chr 16
allele count: 1
allele frequency: 9.218798974869553e-6
allele num: 108474
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+19dupT
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+19dupT
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+19dupT
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.396+19dupT
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.396+19dupT
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.433+19dupT
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+19dupT
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+19dupT
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.469+19dupT
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+19dupT
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21074
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2099
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

16-30012387-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012387
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012387
    reference: chr 16
allele count: 1
allele frequency: 9.279881217520416e-6
allele num: 107760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+26T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+26T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.396+26T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+26T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.469+26T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+26T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.433+26T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+26T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+26T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.396+26T>C
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5720
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

16-30012396-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012396
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012396
    reference: chr 16
allele count: 3
allele frequency: 2.800806632310105e-5
allele num: 107112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.469+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.396+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.396+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+35G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.433+35G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6613
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16917
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3250
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 1.75e1
  variant carriers: 0
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: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

16-30012398-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012398
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012398
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 106874
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+37A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.396+37A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+37A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+37A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.433+37A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+37A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+37A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.396+37A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+37A>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.469+37A>G
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8543
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3634
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3666
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

16-30012402-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012402
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012402
    reference: chr 16
allele count: 1
allele frequency: 9.417259954043771e-6
allele num: 106188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.433+41T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+41T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+41T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+41T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.396+41T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.396+41T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+41T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+41T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.469+41T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+41T>C
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13055
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4565
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

16-30012407-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012407
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012407
    reference: chr 16
allele count: 6
allele frequency: 5.698005698005698e-5
allele num: 105300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.433+46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.396+46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.469+46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+46G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.396+46G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11602
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15480
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6447
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2210
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

16-30012486-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012486
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012486
    reference: chr 16
allele count: 1
allele frequency: 8.21287779237845e-5
allele num: 12176
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+125T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+125T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+125T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+125T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.470-47T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.434-47T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.397-47T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+125T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+125T>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.397-47T>C
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16863
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2496
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

16-30012487-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012487
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012487
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 11824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+126C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+126C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+126C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.470-46C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.397-46C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+126C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.434-46C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+126C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+126C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.397-46C>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32774
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

16-30012490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012490
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012490
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 9850
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+129G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+129G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.434-43G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+129G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+129G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+129G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+129G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.470-43G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.397-43G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.397-43G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14736
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11831
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

16-30012499-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012499
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012499
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 6442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.397-34G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+138G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+138G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+138G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+138G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+138G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+138G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.397-34G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.434-34G>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.470-34G>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10415
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36497
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7063
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

16-30012512-G-GCCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012512
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012516
    reference: chr 16
allele count: 1
allele frequency: 2.305209774089442e-4
allele num: 4338
alternate allele: GCCCC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.397-19_397-16dupCCCC
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+153_396+156dupCCCC
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+153_396+156dupCCCC
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+153_396+156dupCCCC
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.470-19_470-16dupCCCC
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+153_396+156dupCCCC
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+153_70+156dupCCCC
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.434-19_434-16dupCCCC
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.397-19_397-16dupCCCC
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+153_396+156dupCCCC
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35753
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

16-30012515-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012515
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012515
    reference: chr 16
allele count: 1
allele frequency: 2.36854571293226e-4
allele num: 4222
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+154C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.397-18C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+154C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+154C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+154C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.397-18C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.470-18C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.434-18C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+154C>G
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+154C>G
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7188
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5054
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

16-30012522-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012522
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012522
    reference: chr 16
allele count: 1
allele frequency: 2.522704339051463e-4
allele num: 3964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.397-11C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+161C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+161C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+161C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.434-11C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.397-11C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.470-11C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+161C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+161C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+161C>T
  variant of: http://identifiers.org/hgnc/26905
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33671
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2958
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

16-30012531-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012531
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012531
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 3728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.434-2A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.397-2A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+170A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.470-2A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+170A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.397-2A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+170A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+170A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+170A>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+170A>T
  variant of: http://identifiers.org/hgnc/26905
canonical: false
consequence: splice acceptor
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30590
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3819
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
hgvs: n.470-2A>T
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

16-30012537-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012537
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012537
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 3628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.70+176G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.396+176G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.401G>A
  hgvsp: ENSP00000454665.1:p.Arg134Gln
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+176G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+176G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.401G>A
  hgvsp: ENSP00000456073.1:p.Arg134Gln
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.438G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.396+176G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.474G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.396+176G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29066
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg134Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

16-30012571-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012571
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012571
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 3784
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.*21G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.508G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.397-164G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.*21G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+210G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.71-164G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.396+210G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.472G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.397-164G>C
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.397-164G>C
  variant of: http://identifiers.org/hgnc/26905
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4367
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

16-30012583-CTGCTGCCCGGCCCTTCTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012583
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012565
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 3852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25075
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2736
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: CTGCTGCCCGGCCCTTCTG
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

16-30012691-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012691
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012691
    reference: chr 16
allele count: 2795
allele frequency: 1.063951275218881e-1
allele num: 26270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.397-95C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+330C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.397-44C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.628C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.*141C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.71-44C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.397-44C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.592C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.*141C>T
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.397-44C>T
  variant of: http://identifiers.org/hgnc/26905
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 3.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 1.25e1
  variant carriers: 1046
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 24806
  bin: 7.5e0
  variant carriers: 2857
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 2.75e1
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 20353
  bin: 2.5e0
  variant carriers: 480
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 2.25e1
  variant carriers: 293
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 1.75e1
  variant carriers: 402
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 8.75e1
  variant carriers: 227
genotype quality: GenotypeQuality
  all individuals: 12297
  bin: 2.25e1
  variant carriers: 299
genotype quality: GenotypeQuality
  all individuals: 2121
  bin: 6.25e1
  variant carriers: 232
num of homozygotes: 246
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

16-30012692-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012692
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012692
    reference: chr 16
allele count: 2
allele frequency: 7.664597225415804e-5
allele num: 26094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.*142G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+331G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.397-94G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.*142G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.397-43G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.629G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.397-43G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.71-43G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.593G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.397-43G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20851
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2559
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

16-30012693-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012693
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012693
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 26254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000569957
  gene symbol: INO80E
  hgvsc: ENST00000569957.1:n.630G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000457016
  ensembl transcript: ENST00000563197
  gene symbol: INO80E
  hgvsc: ENST00000563197.1:c.397-42G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454924
  ensembl transcript: ENST00000567705
  gene symbol: INO80E
  hgvsc: ENST00000567705.1:c.397-93G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000456073
  ensembl transcript: ENST00000562441
  gene symbol: INO80E
  hgvsc: ENST00000562441.1:c.*143G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000458392
  ensembl transcript: ENST00000562291
  gene symbol: INO80E
  hgvsc: ENST00000562291.2:c.71-42G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000454665
  ensembl transcript: ENST00000567065
  gene symbol: INO80E
  hgvsc: ENST00000567065.1:c.*143G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000459432
  ensembl transcript: ENST00000567987
  gene symbol: INO80E
  hgvsc: ENST00000567987.1:c.397-42G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  hgvsc: ENST00000304516.7:c.396+332G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  hgvsc: ENST00000567254.1:c.397-42G>A
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000169592
  ensembl transcript: ENST00000540562
  gene symbol: INO80E
  hgvsc: ENST00000540562.1:n.594G>A
  variant of: http://identifiers.org/hgnc/26905
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25108
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1976
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

16-30012694-TCCATTCCGCCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30012694
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30012682
    reference: chr 16
allele count: 1
allele frequency: 3.787018101946527e-5
allele num: 26406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000303977
  ensembl transcript: ENST00000304516
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000169592
  ensembl protein: ENSP00000461808
  ensembl transcript: ENST00000567254
  gene symbol: INO80E
  variant of: http://identifiers.org/hgnc/26905
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
num of homozygotes: 0
reference allele: TCCATTCCGCCTC

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2700
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2789
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1865
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 94
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502810255177181e-5
allele num: 66542
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.225e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.446e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.608145e6

GenotypeQuality
all individuals: 2785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1565
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 106
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8608
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2695
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40602
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 9.75e1
variant carriers: 9

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

South Asian
type: Population
allele count: 2
allele frequency: 1.212121212121212e-4
allele num: 16500
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.473830477072719e-4
allele num: 8636
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.013229104028864e-5
allele num: 66520
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.36e1

MQRankSum
type: SiteQuality
SIO_000300: -2.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.745e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-2

DP
type: SiteQuality
SIO_000300: 1.609222e6

GenotypeQuality
all individuals: 2676
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 9.75e1
variant carriers: 93

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

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2776
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40603
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8610
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 55
allele frequency: 8.333333333333333e-3
allele num: 6600
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 37
allele frequency: 5.561902471288557e-4
allele num: 66524
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.648784253184099e-5
allele num: 10364
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

FS
type: SiteQuality
SIO_000300: 1.769e0

VQSLOD
type: SiteQuality
SIO_000300: 3.11e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e-1

DP
type: SiteQuality
SIO_000300: 1.610756e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 1.255e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-1

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

GenotypeQuality
all individuals: 656
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1549
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2672
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8647
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503442884204829e-5
allele num: 66514
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 6.018e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.345e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.608901e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e0

QD
type: SiteQuality
SIO_000300: 1.171e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

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

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2672
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 817
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8647
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
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: 8636
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66514
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e0

FS
type: SiteQuality
SIO_000300: 6.018e0

DP
type: SiteQuality
SIO_000300: 1.608901e6

QD
type: SiteQuality
SIO_000300: 1.171e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.345e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40179
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2758
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8577
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1540
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 12
allele frequency: 1.389210465385506e-3
allele num: 8638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66504
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

DP
type: SiteQuality
SIO_000300: 1.609323e6

QD
type: SiteQuality
SIO_000300: 1.481e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

FS
type: SiteQuality
SIO_000300: 5.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.32e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeQuality
all individuals: 654
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2760
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40289
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 186
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8577
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2660
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66508
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

FS
type: SiteQuality
SIO_000300: 7.843e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.113e-1

MQRankSum
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MQ
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QD
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.475e0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

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

Other
type: Population
allele count: 2
allele frequency: 2.222222222222222e-3
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66496
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MQRankSum
type: SiteQuality
SIO_000300: 7.15e-1

FS
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SIO_000300: 1.411e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.75e-1

QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.2e-1

DP
type: SiteQuality
SIO_000300: 1.609638e6

VQSLOD
type: SiteQuality
SIO_000300: 6.25e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.479e0

GenotypeQuality
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GenotypeQuality
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variant carriers: 206

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 38
allele frequency: 4.401204540189946e-3
allele num: 8634
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504030802550836e-5
allele num: 66488
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
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allele count: 9
allele frequency: 8.690614136732329e-4
allele num: 10356
num of homozygotes: 0

Latino
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allele count: 159
allele frequency: 1.375908618899273e-2
allele num: 11556
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16500
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.665e1

QD
type: SiteQuality
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MQRankSum
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SIO_000300: -1.026e0

InbreedingCoeff
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SIO_000300: 1.02e-2

VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.61183e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.46e-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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66342
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.213444970270598e-4
allele num: 16482
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e0

FS
type: SiteQuality
SIO_000300: 3.317e0

DP
type: SiteQuality
SIO_000300: 1.60067e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 0.0e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.09e-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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South Asian
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allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016682252858306e-5
allele num: 66298
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.08e-1

DP
type: SiteQuality
SIO_000300: 1.598371e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.46e-1

FS
type: SiteQuality
SIO_000300: 6.044e0

MQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.648e1

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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.110975311659741e-5
allele num: 16364
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African
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allele count: 3
allele frequency: 2.909231962761831e-4
allele num: 10312
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.511350240304688e-5
allele num: 66166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

VQSLOD
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InbreedingCoeff
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16228
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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Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.515335192144502e-5
allele num: 65992
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African
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East Asian
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MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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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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variant carriers: 0

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

Other
type: Population
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South Asian
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allele frequency: 1.684341859014348e-3
allele num: 16030
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East Asian
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Latino
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allele frequency: 0.0e0
allele num: 11544
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65792
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African
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.77e-1

DP
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

South Asian
type: Population
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allele frequency: 6.264879087833605e-5
allele num: 15962
num of homozygotes: 0

Other
type: Population
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65714
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Other
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FS
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MQ
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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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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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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Latino
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South Asian
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FS
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MQRankSum
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MQ
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ReadPosRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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Latino
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European (Non-Finnish)
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African
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East Asian
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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DP
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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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European (Non-Finnish)
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Other
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African
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Latino
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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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ReadPosRankSum
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BaseQRankSum
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FS
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DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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South Asian
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European (Non-Finnish)
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European (Finnish)
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allele frequency: 1.515151515151515e-4
allele num: 6600
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Latino
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ClippingRankSum
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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FS
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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Other
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DP
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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QD
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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FS
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DP
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BaseQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10150
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530643482520051e-5
allele num: 65332
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 1.6269e1

QD
type: SiteQuality
SIO_000300: 1.45e1

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.402e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

DP
type: SiteQuality
SIO_000300: 1.553671e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37881
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1809
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2585
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14684
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10150
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73370319001387e-4
allele num: 11536
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.553671e6

FS
type: SiteQuality
SIO_000300: 1.6269e1

VQSLOD
type: SiteQuality
SIO_000300: -2.402e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

QD
type: SiteQuality
SIO_000300: 1.45e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.85e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37783
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7871
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.129141000888725e-5
allele num: 65262
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14582
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.325e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

DP
type: SiteQuality
SIO_000300: 1.550767e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.204e1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

GenotypeQuality
all individuals: 2575
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37196
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2489
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variant carriers: 0

GenotypeQuality
all individuals: 1806
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1497
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4061
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13812
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64980
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.537237e6

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.916e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

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

GenotypeQuality
all individuals: 1915
bin: 9.75e1
variant carriers: 130

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

GenotypeQuality
all individuals: 233
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2462
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2544
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7624
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3868
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 320
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35544
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.737317581653926e-4
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 85
allele frequency: 1.322710155301733e-3
allele num: 64262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 41
allele frequency: 6.208358570563295e-3
allele num: 6604
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.475247524752475e-3
allele num: 808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11900
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: 10000
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.22e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

FS
type: SiteQuality
SIO_000300: 5.37e-1

QD
type: SiteQuality
SIO_000300: 1.185e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

DP
type: SiteQuality
SIO_000300: 1.515304e6

GenotypeQuality
all individuals: 1490
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3961
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7651
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1802
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 627
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.330459100442787e-4
allele num: 8582
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: 11512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.556129594472628e-5
allele num: 64262
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 8.399126490844952e-5
allele num: 11906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
SIO_000300: 1.508561e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 6.218e0

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.96e-1

QD
type: SiteQuality
SIO_000300: 1.07e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2553
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 312
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1802
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3961
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 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: 11512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64262
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.67982529816899e-4
allele num: 11906
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.07e1

FS
type: SiteQuality
SIO_000300: 6.218e0

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

DP
type: SiteQuality
SIO_000300: 1.508561e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7651
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2553
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1490
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1802
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 627
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
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: 10000
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.556129594472628e-5
allele num: 64262
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.07e1

DP
type: SiteQuality
SIO_000300: 1.508561e6

FS
type: SiteQuality
SIO_000300: 6.218e0

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

GenotypeQuality
all individuals: 509
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35679
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2475
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3692
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1803
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 787
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7647
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.00080064051241e-4
allele num: 9992
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64046
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.502944e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.439e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.6e0

GenotypeQuality
all individuals: 2452
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 27

GenotypeQuality
all individuals: 493
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11144
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: 3
allele frequency: 2.609149417289963e-4
allele num: 11498
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.006018054162487e-4
allele num: 9970
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 3.282275711159737e-4
allele num: 63980
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 1.508285e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.32e-1

FS
type: SiteQuality
SIO_000300: 2.526e0

QD
type: SiteQuality
SIO_000300: 1.004e1

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2532
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1892
bin: 9.75e1
variant carriers: 79

GenotypeQuality
all individuals: 279
bin: 3.75e1
variant carriers: 1

African
type: Population
allele count: 2
allele frequency: 2.006018054162487e-4
allele num: 9970
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.609149417289963e-4
allele num: 11498
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 74
allele frequency: 1.156611441075336e-3
allele num: 63980
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11144
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.32e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

DP
type: SiteQuality
SIO_000300: 1.508285e6

FS
type: SiteQuality
SIO_000300: 2.526e0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 1.004e1

GenotypeQuality
all individuals: 7668
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35785
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variant carriers: 0

GenotypeQuality
all individuals: 1803
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GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 786
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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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variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.000200040008002e-4
allele num: 9998
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64020
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.868e0

MQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.224e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 1.502453e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

FS
type: SiteQuality
SIO_000300: 1.6216e1

MQ
type: SiteQuality
SIO_000300: 5.932e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.149e1

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

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
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variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 265
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variant carriers: 0

GenotypeQuality
all individuals: 470
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GenotypeQuality
all individuals: 7668
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variant carriers: 0

GenotypeQuality
all individuals: 2471
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variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.75e1
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GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 1804
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GenotypeQuality
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GenotypeQuality
all individuals: 332
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GenotypeQuality
all individuals: 785
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variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 8.968609865470852e-5
allele num: 11150
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.478e1

FS
type: SiteQuality
SIO_000300: 6.697e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.048e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

DP
type: SiteQuality
SIO_000300: 1.502842e6

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

GenotypeQuality
all individuals: 616
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 147
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
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GenotypeQuality
all individuals: 7522
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 226
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variant carriers: 1

GenotypeQuality
all individuals: 1698
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variant carriers: 1

GenotypeQuality
all individuals: 202
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variant carriers: 1

GenotypeQuality
all individuals: 1522
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 8.25e1
variant carriers: 2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 428
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variant carriers: 0

GenotypeQuality
all individuals: 35541
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variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.934744659916844e-5
allele num: 63014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.641089108910891e-4
allele num: 6464
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.099173553719008e-4
allele num: 9680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.43e-1

FS
type: SiteQuality
SIO_000300: 2.30681e2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.698e0

QD
type: SiteQuality
SIO_000300: 1.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.539e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.855e0

MQ
type: SiteQuality
SIO_000300: 5.937e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

DP
type: SiteQuality
SIO_000300: 1.519756e6

GenotypeQuality
all individuals: 94
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7742
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 36609
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GenotypeQuality
all individuals: 757
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 618
bin: 8.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.707767328456984e-5
allele num: 11484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63702
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.634e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

QD
type: SiteQuality
SIO_000300: 1.346e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.500883e6

VQSLOD
type: SiteQuality
SIO_000300: -2.989e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.84e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2459
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.710801393728223e-5
allele num: 11480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63600
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9852
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.799e1

DP
type: SiteQuality
SIO_000300: 1.498994e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.168e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.129e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
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GenotypeQuality
all individuals: 249
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 37
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GenotypeQuality
all individuals: 405
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GenotypeQuality
all individuals: 617
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GenotypeQuality
all individuals: 751
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GenotypeQuality
all individuals: 1470
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 36383
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variant carriers: 0

GenotypeQuality
all individuals: 1746
bin: 9.75e1
variant carriers: 1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63408
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9948
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.170411985018727e-4
allele num: 8544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.116e1

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.18e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

DP
type: SiteQuality
SIO_000300: 1.494887e6

FS
type: SiteQuality
SIO_000300: 3.604e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-2

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

GenotypeQuality
all individuals: 2449
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 405
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1761
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36383
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1746
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3381
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7716
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.462528387585163e-5
allele num: 63408
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.005227181342983e-4
allele num: 9948
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.18e-1

FS
type: SiteQuality
SIO_000300: 3.604e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.63e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

DP
type: SiteQuality
SIO_000300: 1.494887e6

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

QD
type: SiteQuality
SIO_000300: 1.116e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-2

GenotypeQuality
all individuals: 3415
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 257
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7679
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1753
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2439
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1910
bin: 9.75e1
variant carriers: 199

GenotypeQuality
all individuals: 745
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 36268
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 22
allele frequency: 1.917712691771269e-3
allele num: 11472
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 169
allele frequency: 2.665867432249109e-3
allele num: 63394
num of homozygotes: 1

African
type: Population
allele count: 4
allele frequency: 4.025764895330113e-4
allele num: 9936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.062443164595332e-4
allele num: 6598
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.551020408163265e-3
allele num: 784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.272e1

FS
type: SiteQuality
SIO_000300: 1.168e0

DP
type: SiteQuality
SIO_000300: 1.50401e6

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

MQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.158e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.32e-1

GenotypeQuality
all individuals: 207
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 749
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1458
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2517
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36211
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9884
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: 784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.745483881173084e-5
allele num: 63218
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

QD
type: SiteQuality
SIO_000300: 1.397e1

MQRankSum
type: SiteQuality
SIO_000300: -1.24e-1

FS
type: SiteQuality
SIO_000300: 1.713e0

VQSLOD
type: SiteQuality
SIO_000300: 9.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 1.490797e6

GenotypeQuality
all individuals: 36162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2498
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1674
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3995
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1843
bin: 9.75e1
variant carriers: 142

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7648
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 135
allele frequency: 1.581537019681349e-2
allele num: 8536
num of homozygotes: 1

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

African
type: Population
allele count: 3
allele frequency: 3.03828235770711e-4
allele num: 9874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.911893157794797e-5
allele num: 63196
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.028383381324558e-4
allele num: 9724
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 1.49889e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

FS
type: SiteQuality
SIO_000300: 1.917e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

QD
type: SiteQuality
SIO_000300: 1.469e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1711
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1652
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 36170
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7669
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variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4183
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2434
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2503
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63136
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.171508903467666e-4
allele num: 8536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.59e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

DP
type: SiteQuality
SIO_000300: 1.488461e6

FS
type: SiteQuality
SIO_000300: 2.3e0

QD
type: SiteQuality
SIO_000300: 1.607e1

MQRankSum
type: SiteQuality
SIO_000300: 4.73e-1

GenotypeDepth
all individuals: 347
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 29
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 414
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7563
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35602
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4607
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1706
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17096018735363e-4
allele num: 8540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.029018316526034e-4
allele num: 9718
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.913e1

FS
type: SiteQuality
SIO_000300: 1.675e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

QD
type: SiteQuality
SIO_000300: 2.192e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

DP
type: SiteQuality
SIO_000300: 1.478439e6

VQSLOD
type: SiteQuality
SIO_000300: -2.248e0

MQRankSum
type: SiteQuality
SIO_000300: -6.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1432
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 4.25e1
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GenotypeQuality
all individuals: 35087
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 1833
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 326
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2469
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4801
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62546
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.172332942555686e-4
allele num: 8530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9670
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 1.921e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.303e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: -8.335e-1

DP
type: SiteQuality
SIO_000300: 1.469986e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 7.38e0

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

GenotypeQuality
all individuals: 2341
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 8.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 1956
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 303
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2439
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7410
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 9.75e1
variant carriers: 14

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.282051282051282e-3
allele num: 780
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.92375517009202e-4
allele num: 62378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.039284971939306e-4
allele num: 9622
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.694e0

VQSLOD
type: SiteQuality
SIO_000300: 5.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

DP
type: SiteQuality
SIO_000300: 1.461438e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2298
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 121
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.040366208905535e-4
allele num: 9612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.824857666698833e-5
allele num: 62178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.516e1

DP
type: SiteQuality
SIO_000300: 1.450653e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.74e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.38e-1

GenotypeQuality
all individuals: 5315
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2420
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 357
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variant carriers: 0

GenotypeQuality
all individuals: 92
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GenotypeQuality
all individuals: 7170
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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
all individuals: 1702
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 890
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.180358829084042e-4
allele num: 8472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62072
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.239e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.189e0

MQRankSum
type: SiteQuality
SIO_000300: 8.98e-1

DP
type: SiteQuality
SIO_000300: 1.440487e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.09e0

GenotypeQuality
all individuals: 504
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1214
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1699
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1802
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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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variant carriers: 0

GenotypeQuality
all individuals: 30062
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 418
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variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.622007396353727e-5
allele num: 61652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9640
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.036e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.89e0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

DP
type: SiteQuality
SIO_000300: 1.397724e6

QD
type: SiteQuality
SIO_000300: 1.214e1

GenotypeQuality
all individuals: 1123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24752
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
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GenotypeQuality
all individuals: 687
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1972
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GenotypeQuality
all individuals: 598
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GenotypeQuality
all individuals: 2075
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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
all individuals: 5929
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GenotypeQuality
all individuals: 1697
bin: 9.75e1
variant carriers: 3

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.091190108191654e-4
allele num: 6470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.630736114281987e-5
allele num: 61322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.91e-1

FS
type: SiteQuality
SIO_000300: 2.785e0

MQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.99e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

DP
type: SiteQuality
SIO_000300: 1.336051e6

GenotypeQuality
all individuals: 2286
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22350
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
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GenotypeQuality
all individuals: 753
bin: 1.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9308
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.312e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.314151e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.27e0

GenotypeQuality
all individuals: 4012
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 739
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60802
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.904719501335708e-5
allele num: 11230
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9422
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -8.71e-1

DP
type: SiteQuality
SIO_000300: 1.280754e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

QD
type: SiteQuality
SIO_000300: 6.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.033e0

VQSLOD
type: SiteQuality
SIO_000300: -1.779e0

GenotypeQuality
all individuals: 4905
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4757
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GenotypeQuality
all individuals: 2277
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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: 2646
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GenotypeQuality
all individuals: 1700
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variant carriers: 6

GenotypeQuality
all individuals: 673
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GenotypeQuality
all individuals: 740
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.973438621679828e-5
allele num: 11144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.973639709539441e-5
allele num: 60318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9152
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.141327623126338e-4
allele num: 9340
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.793e0

VQSLOD
type: SiteQuality
SIO_000300: 2.69e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.260551e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

QD
type: SiteQuality
SIO_000300: 1.32e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7070
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1408
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 5.91715976331361e-4
allele num: 1690
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.789e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-1

DP
type: SiteQuality
SIO_000300: 3.23127e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.809999999999999e-2

FS
type: SiteQuality
SIO_000300: 3.522e0

MQRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-1

QD
type: SiteQuality
SIO_000300: 1.408e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1638
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6874
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1370
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.188e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
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SIO_000300: -6.909999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1222
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5686
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1390
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

InbreedingCoeff
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SIO_000300: -7.47e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.116e1

DP
type: SiteQuality
SIO_000300: 2.97245e5

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 940
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1034
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3538
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

FS
type: SiteQuality
SIO_000300: 1.0789e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.37e-2

QD
type: SiteQuality
SIO_000300: 1.147e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 2.47289e5

VQSLOD
type: SiteQuality
SIO_000300: -1.059e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 1
allele frequency: 3.787878787878788e-3
allele num: 264
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

Latino
type: Population
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: 50
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2290
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-2

DP
type: SiteQuality
SIO_000300: 2.09256e5

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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ClippingRankSum
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SIO_000300: -7.2e-1

MQ
type: SiteQuality
SIO_000300: 5.303e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.7e-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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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 50
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Latino
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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: 4.492362982929021e-4
allele num: 2226
num of homozygotes: 0

East Asian
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.95e-2

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.05e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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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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Latino
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allele frequency: 0.0e0
allele num: 196
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.761904761904762e-4
allele num: 2100
num of homozygotes: 0

Other
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.689e0

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.021e1

MQRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 2.158e0

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-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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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 228
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1990
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African
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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 (Finnish)
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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MQ
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DP
type: SiteQuality
SIO_000300: 1.7457e5

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

GenotypeQuality
all individuals: 3777
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3457
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25817
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 30
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1940
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.001e1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 1.67976e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 20881
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3385
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2072
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.506999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.55213e5

QD
type: SiteQuality
SIO_000300: 1.713e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.97e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19239
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5976
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2182
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.53984e5

QD
type: SiteQuality
SIO_000300: 2.93e0

MQ
type: SiteQuality
SIO_000300: 4.838e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.27e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

GenotypeQuality
all individuals: 452
bin: 4.25e1
variant carriers: 54

GenotypeQuality
all individuals: 6488
bin: 1.75e1
variant carriers: 257

GenotypeQuality
all individuals: 1751
bin: 3.25e1
variant carriers: 137

GenotypeQuality
all individuals: 376
bin: 9.25e1
variant carriers: 297

GenotypeQuality
all individuals: 619
bin: 4.75e1
variant carriers: 67

GenotypeQuality
all individuals: 6130
bin: 1.25e1
variant carriers: 153

GenotypeQuality
all individuals: 253
bin: 7.25e1
variant carriers: 69

GenotypeQuality
all individuals: 4178
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 14866
bin: 7.5e0
variant carriers: 153

GenotypeQuality
all individuals: 240
bin: 7.75e1
variant carriers: 48

GenotypeQuality
all individuals: 982
bin: 3.75e1
variant carriers: 40

GenotypeQuality
all individuals: 3847
bin: 9.75e1
variant carriers: 2979

GenotypeQuality
all individuals: 359
bin: 5.75e1
variant carriers: 222

GenotypeQuality
all individuals: 738
bin: 6.75e1
variant carriers: 182

GenotypeQuality
all individuals: 453
bin: 5.25e1
variant carriers: 142

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 119

GenotypeQuality
all individuals: 2106
bin: 2.75e1
variant carriers: 222

Latino
type: Population
allele count: 88
allele frequency: 8.979591836734693e-2
allele num: 980
num of homozygotes: 4

South Asian
type: Population
allele count: 299
allele frequency: 3.887155486219449e-2
allele num: 7692
num of homozygotes: 10

European (Non-Finnish)
type: Population
allele count: 1273
allele frequency: 1.037658950114118e-1
allele num: 12268
num of homozygotes: 65

East Asian
type: Population
allele count: 13
allele frequency: 1.003086419753086e-2
allele num: 1296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 14
allele frequency: 3.783783783783784e-2
allele num: 370
num of homozygotes: 0

Other
type: Population
allele count: 17
allele frequency: 7.327586206896551e-2
allele num: 232
num of homozygotes: 0

African
type: Population
allele count: 1091
allele frequency: 3.178904428904429e-1
allele num: 3432
num of homozygotes: 167

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 5.49733e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.735e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.78e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 2648
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6601
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2273
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16304
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6634
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15249
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.639881928501148e-4
allele num: 12196
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 988
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.31571e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.26e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.926e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

QD
type: SiteQuality
SIO_000300: 1.443e1

GenotypeQuality
all individuals: 16124
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6465
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2259
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6100
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 16395
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12250
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1008
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7678
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.64e0

MQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.34269e5

VQSLOD
type: SiteQuality
SIO_000300: -2.281e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.52e-2