11-15222466-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15222466
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15222466
    reference: chr 11
allele count: 5
allele frequency: 5.751621957391985e-5
allele num: 86932
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.931G>A
  hgvsp: ENSP00000368872.3:p.Val311Met
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.790G>A
  hgvsp: ENSP00000368874.3:p.Val264Met
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.261+10106G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.693+10106G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.790G>A
  hgvsp: ENSP00000435022.1:p.Val264Met
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.790G>A
  hgvsp: ENSP00000436194.1:p.Val264Met
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.693+10106G>A
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10705
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16587
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2577
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16404
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27692
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2444
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val311Met
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

11-15222498-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15222498
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15222498
    reference: chr 11
allele count: 259
allele frequency: 4.258187557543075e-3
allele num: 60824
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.693+10138A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.819+3A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.960+3A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.693+10138A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.819+3A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.819+3A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.261+10138A>G
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 6594
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17320
  bin: 1.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 22942
  bin: 7.5e0
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 1.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 2.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1339
  bin: 9.75e1
  variant carriers: 242
genotype quality: GenotypeQuality
  all individuals: 2550
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.75e1
  variant carriers: 2
hgvs: c.960+3A>G
num of homozygotes: 8
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

11-15222501-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15222501
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15222501
    reference: chr 11
allele count: 2
allele frequency: 3.479592191795122e-5
allele num: 57478
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.819+6G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.819+6G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.261+10141G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.693+10141G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.819+6G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.693+10141G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.960+6G>A
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7824
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16497
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8229
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31621
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1454
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
hgvs: c.960+6G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

11-15222511-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15222511
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15222511
    reference: chr 11
allele count: 1
allele frequency: 2.072109407376709e-5
allele num: 48260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.693+10151T>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.819+16T>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.693+10151T>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.819+16T>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.960+16T>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.819+16T>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.261+10151T>C
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11792
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13332
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12100
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

11-15222520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15222520
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15222520
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 41688
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.819+25C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.693+10160C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.261+10160C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.819+25C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.960+25C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.693+10160C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.819+25C>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15098
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23413
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2043
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15300
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

11-15222521-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15222521
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15222521
    reference: chr 11
allele count: 1
allele frequency: 2.433800623052959e-5
allele num: 41088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.693+10161C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.819+26C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.819+26C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.693+10161C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.960+26C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.819+26C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.261+10161C>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23352
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10896
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15420
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2061
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22487
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15595
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

11-15222526-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15222526
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15222526
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 38720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.819+31G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.819+31G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.819+31G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.693+10166G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.960+31G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.693+10166G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.261+10166G>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23282
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16614
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20922
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2143
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3091
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4350
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16803
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

11-15222539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15222539
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15222539
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 32830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.819+44G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.819+44G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.960+44G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.693+10179G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.693+10179G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.819+44G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.261+10179G>A
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17751
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24555
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2184
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17465
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

11-15222547-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15222547
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15222547
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 30984
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.693+10187G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.693+10187G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.819+52G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.960+52G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.819+52G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.261+10187G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.819+52G>C
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17793
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24927
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6730
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7330
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16140
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2213
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9090
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3639
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

11-15242973-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15242973
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15242973
    reference: chr 11
allele count: 1
allele frequency: 9.06043308870164e-6
allele num: 110370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.820-50A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.820-50A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.262-50A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.961-50A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.820-50A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.694-50A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.694-50A>G
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25778
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5921
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/11-15242985-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15242985
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15242985
    reference: chr 11
allele count: 1
allele frequency: 9.046826373308244e-6
allele num: 110536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.694-38C>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.820-38C>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.961-38C>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.262-38C>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.820-38C>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.694-38C>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.820-38C>A
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8670
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2868
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5930
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14656
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26150
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ

11-15242998-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15242998
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15242998
    reference: chr 11
allele count: 2
allele frequency: 1.798399424512184e-5
allele num: 111210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.694-25G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.820-25G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.961-25G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.820-25G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.262-25G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.694-25G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.820-25G>A
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3618
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

11-15243006-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243006
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243006
    reference: chr 11
allele count: 2
allele frequency: 1.788141048565911e-5
allele num: 111848
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.820-17C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.961-17C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.694-17C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.820-17C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.262-17C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.820-17C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.694-17C>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1719
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3741
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

11-15243007-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243007
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243007
    reference: chr 11
allele count: 1
allele frequency: 8.932080460180785e-6
allele num: 111956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.820-16C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.694-16C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.820-16C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.961-16C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.820-16C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.262-16C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.694-16C>G
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5965
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3693
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff

11-15243008-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243008
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243008
    reference: chr 11
allele count: 2
allele frequency: 1.78491744756805e-5
allele num: 112050
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.820-15T>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.961-15T>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.820-15T>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.820-15T>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.694-15T>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.262-15T>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.694-15T>G
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3738
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27036
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

11-15243013-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243013
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243013
    reference: chr 11
allele count: 1
allele frequency: 8.89157612078317e-6
allele num: 112466
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.961-10C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.820-10C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.694-10C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.694-10C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.262-10C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.820-10C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.820-10C>G
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14647
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD

11-15243019-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243019
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243019
    reference: chr 11
allele count: 2
allele frequency: 1.769316513031016e-5
allele num: 113038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.820-4G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.262-4G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.694-4G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.961-4G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.694-4G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.820-4G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.820-4G>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1722
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27380
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3634
  bin: 2.25e1
  variant carriers: 0
hgvs: c.961-4G>T
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

11-15243020-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243020
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243020
    reference: chr 11
allele count: 7
allele frequency: 6.189213085764811e-5
allele num: 113100
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.961-3C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.820-3C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.262-3C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.820-3C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.694-3C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.820-3C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.694-3C>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2011
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5999
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
hgvs: c.961-3C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS

11-15243024-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243024
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243024
    reference: chr 11
allele count: 1
allele frequency: 8.793218669761879e-6
allele num: 113724
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.821T>G
  hgvsp: ENSP00000368874.3:p.Val274Gly
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.695T>G
  hgvsp: ENSP00000389161.1:p.Val232Gly
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.263T>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.821T>G
  hgvsp: ENSP00000435022.1:p.Val274Gly
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.821T>G
  hgvsp: ENSP00000436194.1:p.Val274Gly
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.962T>G
  hgvsp: ENSP00000368872.3:p.Val321Gly
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.695T>G
  hgvsp: ENSP00000436113.1:p.Val232Gly
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2011
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27667
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val321Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-15243025-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243025
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243025
    reference: chr 11
allele count: 1
allele frequency: 8.780247954202227e-6
allele num: 113892
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.963G>A
  hgvsp: ENST00000379554.3:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.264G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.696G>A
  hgvsp: ENST00000424273.1:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.696G>A
  hgvsp: ENST00000525218.1:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.822G>A
  hgvsp: ENST00000379556.3:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.822G>A
  hgvsp: ENST00000528567.1:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.822G>A
  hgvsp: ENST00000530161.1:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6016
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27871
  bin: 6.25e1
  variant carriers: 0
hgvs: c.963G>A
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

11-15243031-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243031
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243031
    reference: chr 11
allele count: 2
allele frequency: 1.748343444586255e-5
allele num: 114394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.702C>T
  hgvsp: ENST00000424273.1:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.828C>T
  hgvsp: ENST00000528567.1:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.969C>T
  hgvsp: ENST00000379554.3:c.969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.828C>T
  hgvsp: ENST00000379556.3:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.702C>T
  hgvsp: ENST00000525218.1:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.270C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.828C>T
  hgvsp: ENST00000530161.1:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly323Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD

11-15243032-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243032
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243032
    reference: chr 11
allele count: 19
allele frequency: 1.653180196641434e-4
allele num: 114930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.703G>A
  hgvsp: ENSP00000389161.1:p.Val235Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.703G>A
  hgvsp: ENSP00000436113.1:p.Val235Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.271G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.829G>A
  hgvsp: ENSP00000368874.3:p.Val277Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.829G>A
  hgvsp: ENSP00000436194.1:p.Val277Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.970G>A
  hgvsp: ENSP00000368872.3:p.Val324Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.829G>A
  hgvsp: ENSP00000435022.1:p.Val277Ile
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8439
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2921
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val324Ile
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

11-15243046-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243046
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243046
    reference: chr 11
allele count: 6
allele frequency: 5.131362889983579e-5
allele num: 116928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.843C>T
  hgvsp: ENST00000530161.1:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.843C>T
  hgvsp: ENST00000379556.3:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.717C>T
  hgvsp: ENST00000525218.1:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.285C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.843C>T
  hgvsp: ENST00000528567.1:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.984C>T
  hgvsp: ENST00000379554.3:c.984C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.717C>T
  hgvsp: ENST00000424273.1:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6168
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala328Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-15243047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243047
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243047
    reference: chr 11
allele count: 3433
allele frequency: 2.925087761153335e-2
allele num: 117364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.286G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.718G>A
  hgvsp: ENSP00000436113.1:p.Asp240Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.844G>A
  hgvsp: ENSP00000368874.3:p.Asp282Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.985G>A
  hgvsp: ENSP00000368872.3:p.Asp329Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.844G>A
  hgvsp: ENSP00000436194.1:p.Asp282Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.718G>A
  hgvsp: ENSP00000389161.1:p.Asp240Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.844G>A
  hgvsp: ENSP00000435022.1:p.Asp282Asn
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 7.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 4.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 1.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 5.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 8793
  bin: 3.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 9.75e1
  variant carriers: 1896
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 3.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 5.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 9355
  bin: 2.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 8.25e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.75e1
  variant carriers: 155
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 6.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 20926
  bin: 2.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.75e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 9.25e1
  variant carriers: 162
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29256
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2043
  bin: 7.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 15110
  bin: 9.75e1
  variant carriers: 3339
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp329Asn
num of homozygotes: 76
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-15243049-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243049
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243049
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 117626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.720C>A
  hgvsp: ENSP00000389161.1:p.Asp240Glu
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.720C>A
  hgvsp: ENSP00000436113.1:p.Asp240Glu
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.846C>A
  hgvsp: ENSP00000435022.1:p.Asp282Glu
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.846C>A
  hgvsp: ENSP00000368874.3:p.Asp282Glu
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.987C>A
  hgvsp: ENSP00000368872.3:p.Asp329Glu
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.846C>A
  hgvsp: ENSP00000436194.1:p.Asp282Glu
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.288C>A
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31227
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1877
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2181
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp329Glu
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

11-15243053-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243053
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243053
    reference: chr 11
allele count: 1
allele frequency: 8.461382251404589e-6
allele num: 118184
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.850C>G
  hgvsp: ENSP00000435022.1:p.Leu284Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.724C>G
  hgvsp: ENSP00000436113.1:p.Leu242Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.292C>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.850C>G
  hgvsp: ENSP00000368874.3:p.Leu284Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.991C>G
  hgvsp: ENSP00000368872.3:p.Leu331Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.850C>G
  hgvsp: ENSP00000436194.1:p.Leu284Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.724C>G
  hgvsp: ENSP00000389161.1:p.Leu242Val
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12324
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1369
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu331Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/11-15243056-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243056
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243056
    reference: chr 11
allele count: 2
allele frequency: 1.68713726548792e-5
allele num: 118544
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.853A>C
  hgvsp: ENSP00000435022.1:p.Thr285Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.727A>C
  hgvsp: ENSP00000389161.1:p.Thr243Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.295A>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.853A>C
  hgvsp: ENSP00000436194.1:p.Thr285Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.853A>C
  hgvsp: ENSP00000368874.3:p.Thr285Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.994A>C
  hgvsp: ENSP00000368872.3:p.Thr332Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.727A>C
  hgvsp: ENSP00000436113.1:p.Thr243Pro
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31663
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1301
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1887
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr332Pro
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: A
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

11-15243058-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243058
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243058
    reference: chr 11
allele count: 3
allele frequency: 2.529596276434281e-5
allele num: 118596
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.855C>T
  hgvsp: ENST00000530161.1:c.855C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.729C>T
  hgvsp: ENST00000525218.1:c.729C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.729C>T
  hgvsp: ENST00000424273.1:c.729C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.996C>T
  hgvsp: ENST00000379554.3:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.855C>T
  hgvsp: ENST00000528567.1:c.855C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.297C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.855C>T
  hgvsp: ENST00000379556.3:c.855C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12275
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6604
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1213
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr332Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

11-15243059-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243059
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243059
    reference: chr 11
allele count: 8131
allele frequency: 6.835875102987911e-2
allele num: 118946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.730G>A
  hgvsp: ENSP00000436113.1:p.Asp244Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.298G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.856G>A
  hgvsp: ENSP00000436194.1:p.Asp286Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.730G>A
  hgvsp: ENSP00000389161.1:p.Asp244Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.856G>A
  hgvsp: ENSP00000368874.3:p.Asp286Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.856G>A
  hgvsp: ENSP00000435022.1:p.Asp286Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.997G>A
  hgvsp: ENSP00000368872.3:p.Asp333Asn
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 8.25e1
  variant carriers: 377
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 9.75e1
  variant carriers: 3513
genotype depth: GenotypeDepth
  all individuals: 22707
  bin: 2.75e1
  variant carriers: 302
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 3.75e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.25e1
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 4.25e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 4.75e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9980
  bin: 2.25e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.25e1
  variant carriers: 307
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 1.75e1
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 9.25e1
  variant carriers: 428
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 5.75e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 3.25e1
  variant carriers: 255
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.25e1
  variant carriers: 236
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 7.75e1
  variant carriers: 357
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.75e1
  variant carriers: 293
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 8.75e1
  variant carriers: 410
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 9.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 7.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 31205
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 8.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.25e1
  variant carriers: 4
hgvs: p.Asp333Asn
num of homozygotes: 347
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/11-15243061-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243061
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243061
    reference: chr 11
allele count: 2
allele frequency: 1.680785262874815e-5
allele num: 118992
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.732C>A
  hgvsp: ENSP00000389161.1:p.Asp244Glu
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.732C>A
  hgvsp: ENSP00000436113.1:p.Asp244Glu
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.858C>A
  hgvsp: ENSP00000436194.1:p.Asp286Glu
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.300C>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.858C>A
  hgvsp: ENSP00000435022.1:p.Asp286Glu
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.999C>A
  hgvsp: ENSP00000368872.3:p.Asp333Glu
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.858C>A
  hgvsp: ENSP00000368874.3:p.Asp286Glu
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7516
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp333Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/11-15243063-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243063
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243063
    reference: chr 11
allele count: 143
allele frequency: 1.276557757543296e-3
allele num: 112020
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1001A>C
  hgvsp: ENSP00000368872.3:p.Asn334Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.734A>C
  hgvsp: ENSP00000389161.1:p.Asn245Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.302A>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.860A>C
  hgvsp: ENSP00000436194.1:p.Asn287Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.860A>C
  hgvsp: ENSP00000435022.1:p.Asn287Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.860A>C
  hgvsp: ENSP00000368874.3:p.Asn287Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.734A>C
  hgvsp: ENSP00000436113.1:p.Asn245Thr
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 11085
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 9.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 10611
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 26114
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3439
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 35719
  bin: 6.25e1
  variant carriers: 4
hgvs: p.Asn334Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/11-15243080-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243080
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243080
    reference: chr 11
allele count: 1
allele frequency: 8.348360382020972e-6
allele num: 119784
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.877A>C
  hgvsp: ENSP00000435022.1:p.Thr293Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.751A>C
  hgvsp: ENSP00000389161.1:p.Thr251Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.877A>C
  hgvsp: ENSP00000436194.1:p.Thr293Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1018A>C
  hgvsp: ENSP00000368872.3:p.Thr340Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.319A>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.877A>C
  hgvsp: ENSP00000368874.3:p.Thr293Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.751A>C
  hgvsp: ENSP00000436113.1:p.Thr251Pro
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4899
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8027
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1429
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr340Pro
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-15243082-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243082
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243082
    reference: chr 11
allele count: 1
allele frequency: 8.346548702111677e-6
allele num: 119810
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.879A>G
  hgvsp: ENST00000379556.3:c.879A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.321A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.879A>G
  hgvsp: ENST00000528567.1:c.879A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.879A>G
  hgvsp: ENST00000530161.1:c.879A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.753A>G
  hgvsp: ENST00000525218.1:c.753A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1020A>G
  hgvsp: ENST00000379554.3:c.1020A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.753A>G
  hgvsp: ENST00000424273.1:c.753A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2147
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38765
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr340Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-15243083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243083
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243083
    reference: chr 11
allele count: 2
allele frequency: 1.669476952870666e-5
allele num: 119798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.880C>T
  hgvsp: ENSP00000435022.1:p.Arg294Trp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.880C>T
  hgvsp: ENSP00000368874.3:p.Arg294Trp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1021C>T
  hgvsp: ENSP00000368872.3:p.Arg341Trp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.754C>T
  hgvsp: ENSP00000389161.1:p.Arg252Trp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.754C>T
  hgvsp: ENSP00000436113.1:p.Arg252Trp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.880C>T
  hgvsp: ENSP00000436194.1:p.Arg294Trp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.322C>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38700
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg341Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

11-15243089-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243089
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243089
    reference: chr 11
allele count: 16
allele frequency: 1.33515804933409e-4
allele num: 119836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.886G>A
  hgvsp: ENSP00000435022.1:p.Glu296Lys
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.760G>A
  hgvsp: ENSP00000389161.1:p.Glu254Lys
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.760G>A
  hgvsp: ENSP00000436113.1:p.Glu254Lys
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.328G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1027G>A
  hgvsp: ENSP00000368872.3:p.Glu343Lys
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.886G>A
  hgvsp: ENSP00000368874.3:p.Glu296Lys
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.886G>A
  hgvsp: ENSP00000436194.1:p.Glu296Lys
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11414
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 28069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu343Lys
num of homozygotes: 1
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

11-15243092-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243092
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243092
    reference: chr 11
allele count: 1
allele frequency: 8.347384764353328e-6
allele num: 119798
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.763G>A
  hgvsp: ENSP00000436113.1:p.Ala255Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.889G>A
  hgvsp: ENSP00000368874.3:p.Ala297Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1030G>A
  hgvsp: ENSP00000368872.3:p.Ala344Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.763G>A
  hgvsp: ENSP00000389161.1:p.Ala255Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.889G>A
  hgvsp: ENSP00000436194.1:p.Ala297Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.331G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.889G>A
  hgvsp: ENSP00000435022.1:p.Ala297Thr
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala344Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

11-15243093-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243093
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243093
    reference: chr 11
allele count: 1
allele frequency: 8.346688034188035e-6
allele num: 119808
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1031C>T
  hgvsp: ENSP00000368872.3:p.Ala344Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.890C>T
  hgvsp: ENSP00000436194.1:p.Ala297Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.890C>T
  hgvsp: ENSP00000435022.1:p.Ala297Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.332C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.764C>T
  hgvsp: ENSP00000389161.1:p.Ala255Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.764C>T
  hgvsp: ENSP00000436113.1:p.Ala255Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.890C>T
  hgvsp: ENSP00000368874.3:p.Ala297Val
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4877
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala344Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-15243096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243096
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243096
    reference: chr 11
allele count: 10
allele frequency: 8.34752412434472e-5
allele num: 119796
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1034C>T
  hgvsp: ENSP00000368872.3:p.Ala345Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.767C>T
  hgvsp: ENSP00000436113.1:p.Ala256Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.893C>T
  hgvsp: ENSP00000368874.3:p.Ala298Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.893C>T
  hgvsp: ENSP00000436194.1:p.Ala298Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.893C>T
  hgvsp: ENSP00000435022.1:p.Ala298Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.767C>T
  hgvsp: ENSP00000389161.1:p.Ala256Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.335C>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28034
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11414
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38741
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4877
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala345Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

11-15243097-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243097
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243097
    reference: chr 11
allele count: 112
allele frequency: 9.35094427839097e-4
allele num: 119774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.336G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.894G>A
  hgvsp: ENST00000530161.1:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.894G>A
  hgvsp: ENST00000379556.3:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.768G>A
  hgvsp: ENST00000525218.1:c.768G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.768G>A
  hgvsp: ENST00000424273.1:c.768G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.894G>A
  hgvsp: ENST00000528567.1:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1035G>A
  hgvsp: ENST00000379554.3:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28043
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8004
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38727
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala345Ala
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-15243098-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243098
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243098
    reference: chr 11
allele count: 2
allele frequency: 1.669699954918101e-5
allele num: 119782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.337G>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.895G>T
  hgvsp: ENSP00000436194.1:p.Ala299Ser
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.769G>T
  hgvsp: ENSP00000436113.1:p.Ala257Ser
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.895G>T
  hgvsp: ENSP00000435022.1:p.Ala299Ser
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.769G>T
  hgvsp: ENSP00000389161.1:p.Ala257Ser
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1036G>T
  hgvsp: ENSP00000368872.3:p.Ala346Ser
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.895G>T
  hgvsp: ENSP00000368874.3:p.Ala299Ser
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8022
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4769
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala346Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

11-15243107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243107
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243107
    reference: chr 11
allele count: 1
allele frequency: 8.346688034188035e-6
allele num: 119808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.346G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.778G>A
  hgvsp: ENSP00000389161.1:p.Ala260Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.904G>A
  hgvsp: ENSP00000368874.3:p.Ala302Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.778G>A
  hgvsp: ENSP00000436113.1:p.Ala260Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.904G>A
  hgvsp: ENSP00000435022.1:p.Ala302Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1045G>A
  hgvsp: ENSP00000368872.3:p.Ala349Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.904G>A
  hgvsp: ENSP00000436194.1:p.Ala302Thr
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39051
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4752
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala349Thr
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/11-15243111-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243111
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243111
    reference: chr 11
allele count: 1
allele frequency: 8.349196807267141e-6
allele num: 119772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.908A>C
  hgvsp: ENSP00000435022.1:p.Gln303Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1049A>C
  hgvsp: ENSP00000368872.3:p.Gln350Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.350A>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.908A>C
  hgvsp: ENSP00000436194.1:p.Gln303Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.908A>C
  hgvsp: ENSP00000368874.3:p.Gln303Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.782A>C
  hgvsp: ENSP00000389161.1:p.Gln261Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.782A>C
  hgvsp: ENSP00000436113.1:p.Gln261Pro
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln350Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

11-15243114-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243114
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243114
    reference: chr 11
allele count: 6
allele frequency: 5.011359080582654e-5
allele num: 119728
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.911T>C
  hgvsp: ENSP00000368874.3:p.Val304Ala
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.353T>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1052T>C
  hgvsp: ENSP00000368872.3:p.Val351Ala
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.785T>C
  hgvsp: ENSP00000436113.1:p.Val262Ala
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.785T>C
  hgvsp: ENSP00000389161.1:p.Val262Ala
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.911T>C
  hgvsp: ENSP00000435022.1:p.Val304Ala
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.911T>C
  hgvsp: ENSP00000436194.1:p.Val304Ala
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val351Ala
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/11-15243116-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243116
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243116
    reference: chr 11
allele count: 6
allele frequency: 5.015212812196997e-5
allele num: 119636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.913A>C
  hgvsp: ENSP00000368874.3:p.Thr305Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.913A>C
  hgvsp: ENSP00000436194.1:p.Thr305Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.913A>C
  hgvsp: ENSP00000435022.1:p.Thr305Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1054A>C
  hgvsp: ENSP00000368872.3:p.Thr352Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.787A>C
  hgvsp: ENSP00000389161.1:p.Thr263Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.787A>C
  hgvsp: ENSP00000436113.1:p.Thr263Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.355A>C
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38657
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4738
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr352Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

11-15243119-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243119
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243119
    reference: chr 11
allele count: 6
allele frequency: 5.013368983957219e-5
allele num: 119680
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1057T>C
  hgvsp: ENSP00000368872.3:p.Ser353Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.358T>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.916T>C
  hgvsp: ENSP00000435022.1:p.Ser306Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.916T>C
  hgvsp: ENSP00000368874.3:p.Ser306Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.790T>C
  hgvsp: ENSP00000436113.1:p.Ser264Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.790T>C
  hgvsp: ENSP00000389161.1:p.Ser264Pro
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.916T>C
  hgvsp: ENSP00000436194.1:p.Ser306Pro
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38923
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2344
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser353Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS

11-15243120-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243120
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243120
    reference: chr 11
allele count: 1
allele frequency: 8.354916868577158e-6
allele num: 119690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.791C>T
  hgvsp: ENSP00000436113.1:p.Ser264Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.359C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.917C>T
  hgvsp: ENSP00000435022.1:p.Ser306Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.791C>T
  hgvsp: ENSP00000389161.1:p.Ser264Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.917C>T
  hgvsp: ENSP00000368874.3:p.Ser306Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.917C>T
  hgvsp: ENSP00000436194.1:p.Ser306Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1058C>T
  hgvsp: ENSP00000368872.3:p.Ser353Phe
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11774
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39007
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7946
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2341
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser353Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

11-15243122-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243122
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243122
    reference: chr 11
allele count: 9
allele frequency: 7.524077046548956e-5
allele num: 119616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.919C>T
  hgvsp: ENSP00000368874.3:p.Pro307Ser
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.361C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.919C>T
  hgvsp: ENSP00000435022.1:p.Pro307Ser
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.793C>T
  hgvsp: ENSP00000436113.1:p.Pro265Ser
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1060C>T
  hgvsp: ENSP00000368872.3:p.Pro354Ser
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.919C>T
  hgvsp: ENSP00000436194.1:p.Pro307Ser
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.793C>T
  hgvsp: ENSP00000389161.1:p.Pro265Ser
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28142
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2338
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4727
  bin: 9.75e1
  variant carriers: 9
hgvs: p.Pro354Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

11-15243125-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243125
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243125
    reference: chr 11
allele count: 5
allele frequency: 4.18025248725023e-5
allele num: 119610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.796C>T
  hgvsp: ENSP00000436113.1:p.His266Tyr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.922C>T
  hgvsp: ENSP00000436194.1:p.His308Tyr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.922C>T
  hgvsp: ENSP00000368874.3:p.His308Tyr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.796C>T
  hgvsp: ENSP00000389161.1:p.His266Tyr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.922C>T
  hgvsp: ENSP00000435022.1:p.His308Tyr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.364C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1063C>T
  hgvsp: ENSP00000368872.3:p.His355Tyr
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His355Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-15243127-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243127
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243127
    reference: chr 11
allele count: 1
allele frequency: 8.360644772924887e-6
allele num: 119608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.924C>A
  hgvsp: ENSP00000368874.3:p.His308Gln
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.924C>A
  hgvsp: ENSP00000435022.1:p.His308Gln
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.924C>A
  hgvsp: ENSP00000436194.1:p.His308Gln
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1065C>A
  hgvsp: ENSP00000368872.3:p.His355Gln
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.798C>A
  hgvsp: ENSP00000436113.1:p.His266Gln
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.798C>A
  hgvsp: ENSP00000389161.1:p.His266Gln
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.366C>A
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His355Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

11-15243133-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243133
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243133
    reference: chr 11
allele count: 2
allele frequency: 1.67313612635524e-5
allele num: 119536
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.372C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1071C>T
  hgvsp: ENST00000379554.3:c.1071C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.930C>T
  hgvsp: ENST00000528567.1:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.930C>T
  hgvsp: ENST00000530161.1:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.804C>T
  hgvsp: ENST00000424273.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.930C>T
  hgvsp: ENST00000379556.3:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.804C>T
  hgvsp: ENST00000525218.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro357Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-15243134-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243134
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243134
    reference: chr 11
allele count: 12
allele frequency: 1.004083271972689e-4
allele num: 119512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.931G>A
  hgvsp: ENSP00000435022.1:p.Val311Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1072G>A
  hgvsp: ENSP00000368872.3:p.Val358Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.931G>A
  hgvsp: ENSP00000436194.1:p.Val311Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.805G>A
  hgvsp: ENSP00000389161.1:p.Val269Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.805G>A
  hgvsp: ENSP00000436113.1:p.Val269Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.373G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.931G>A
  hgvsp: ENSP00000368874.3:p.Val311Ile
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7907
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val358Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

11-15243158-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243158
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243158
    reference: chr 11
allele count: 3
allele frequency: 2.522195318805488e-5
allele num: 118944
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.955C>G
  hgvsp: ENSP00000436194.1:p.Leu319Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.955C>G
  hgvsp: ENSP00000368874.3:p.Leu319Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1096C>G
  hgvsp: ENSP00000368872.3:p.Leu366Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.829C>G
  hgvsp: ENSP00000436113.1:p.Leu277Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.955C>G
  hgvsp: ENSP00000435022.1:p.Leu319Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.829C>G
  hgvsp: ENSP00000389161.1:p.Leu277Val
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.397C>G
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11051
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38557
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu366Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-15243166-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243166
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243166
    reference: chr 11
allele count: 2
allele frequency: 1.688818333811832e-5
allele num: 118426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.405C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.837C>T
  hgvsp: ENST00000424273.1:c.837C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.963C>T
  hgvsp: ENST00000528567.1:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.837C>T
  hgvsp: ENST00000525218.1:c.837C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1104C>T
  hgvsp: ENST00000379554.3:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.963C>T
  hgvsp: ENST00000379556.3:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.963C>T
  hgvsp: ENST00000530161.1:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4663
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2215
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser368Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

11-15243168-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243168
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243168
    reference: chr 11
allele count: 1
allele frequency: 8.454943605526151e-6
allele num: 118274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.965T>C
  hgvsp: ENSP00000368874.3:p.Met322Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1106T>C
  hgvsp: ENSP00000368872.3:p.Met369Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.965T>C
  hgvsp: ENSP00000435022.1:p.Met322Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.407T>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.965T>C
  hgvsp: ENSP00000436194.1:p.Met322Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.839T>C
  hgvsp: ENSP00000436113.1:p.Met280Thr
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.839T>C
  hgvsp: ENSP00000389161.1:p.Met280Thr
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10915
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4660
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met369Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

11-15243176-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243176
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243176
    reference: chr 11
allele count: 3
allele frequency: 2.553756575923183e-5
allele num: 117474
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.973A>T
  hgvsp: ENSP00000436194.1:p.Ile325Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.847A>T
  hgvsp: ENSP00000389161.1:p.Ile283Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.415A>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.973A>T
  hgvsp: ENSP00000368874.3:p.Ile325Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1114A>T
  hgvsp: ENSP00000368872.3:p.Ile372Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.973A>T
  hgvsp: ENSP00000435022.1:p.Ile325Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.847A>T
  hgvsp: ENSP00000436113.1:p.Ile283Phe
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36707
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4655
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2837
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile372Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

11-15243177-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243177
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243177
    reference: chr 11
allele count: 1
allele frequency: 8.520064752492119e-6
allele num: 117370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.974T>A
  hgvsp: ENSP00000435022.1:p.Ile325Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.848T>A
  hgvsp: ENSP00000389161.1:p.Ile283Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.974T>A
  hgvsp: ENSP00000368874.3:p.Ile325Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.974T>A
  hgvsp: ENSP00000436194.1:p.Ile325Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1115T>A
  hgvsp: ENSP00000368872.3:p.Ile372Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.848T>A
  hgvsp: ENSP00000436113.1:p.Ile283Asn
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.416T>A
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36485
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2918
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7430
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile372Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

11-15243178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243178
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243178
    reference: chr 11
allele count: 2
allele frequency: 1.70826286749005e-5
allele num: 117078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.975C>T
  hgvsp: ENST00000528567.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.417C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.975C>T
  hgvsp: ENST00000379556.3:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1116C>T
  hgvsp: ENST00000379554.3:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.849C>T
  hgvsp: ENST00000424273.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.849C>T
  hgvsp: ENST00000525218.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.975C>T
  hgvsp: ENST00000530161.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36039
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile372Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-15243179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243179
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243179
    reference: chr 11
allele count: 274
allele frequency: 2.340480054668147e-3
allele num: 117070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.850G>A
  hgvsp: ENSP00000389161.1:p.Val284Met
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.976G>A
  hgvsp: ENSP00000368874.3:p.Val326Met
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.850G>A
  hgvsp: ENSP00000436113.1:p.Val284Met
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1117G>A
  hgvsp: ENSP00000368872.3:p.Val373Met
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.976G>A
  hgvsp: ENSP00000435022.1:p.Val326Met
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.418G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.976G>A
  hgvsp: ENSP00000436194.1:p.Val326Met
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 10273
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10671
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26948
  bin: 2.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 7357
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4750
  bin: 9.75e1
  variant carriers: 270
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val373Met
num of homozygotes: 3
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

11-15243181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243181
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243181
    reference: chr 11
allele count: 4
allele frequency: 3.435186616512942e-5
allele num: 116442
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.420G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.978G>A
  hgvsp: ENST00000379556.3:c.978G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.978G>A
  hgvsp: ENST00000530161.1:c.978G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.852G>A
  hgvsp: ENST00000424273.1:c.852G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1119G>A
  hgvsp: ENST00000379554.3:c.1119G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.978G>A
  hgvsp: ENST00000528567.1:c.978G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.852G>A
  hgvsp: ENST00000525218.1:c.852G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35308
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val373Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

11-15243182-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243182
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243182
    reference: chr 11
allele count: 1
allele frequency: 8.587819037477242e-6
allele num: 116444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.853A>G
  hgvsp: ENSP00000436113.1:p.Thr285Ala
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.853A>G
  hgvsp: ENSP00000389161.1:p.Thr285Ala
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1120A>G
  hgvsp: ENSP00000368872.3:p.Thr374Ala
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.979A>G
  hgvsp: ENSP00000436194.1:p.Thr327Ala
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.421A>G
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.979A>G
  hgvsp: ENSP00000435022.1:p.Thr327Ala
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.979A>G
  hgvsp: ENSP00000368874.3:p.Thr327Ala
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4482
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr374Ala
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/11-15243184-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243184
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243184
    reference: chr 11
allele count: 1
allele frequency: 8.619649352664333e-6
allele num: 116014
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1122A>C
  hgvsp: ENST00000379554.3:c.1122A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.423A>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.981A>C
  hgvsp: ENST00000530161.1:c.981A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.855A>C
  hgvsp: ENST00000525218.1:c.855A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.855A>C
  hgvsp: ENST00000424273.1:c.855A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.981A>C
  hgvsp: ENST00000528567.1:c.981A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.981A>C
  hgvsp: ENST00000379556.3:c.981A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10415
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26388
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3834
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4481
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34748
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr374Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-15243186-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243186
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243186
    reference: chr 11
allele count: 4
allele frequency: 3.450893781489406e-5
allele num: 115912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.857C>A
  hgvsp: ENSP00000389161.1:p.Ala286Asp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1124C>A
  hgvsp: ENSP00000368872.3:p.Ala375Asp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.983C>A
  hgvsp: ENSP00000435022.1:p.Ala328Asp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.857C>A
  hgvsp: ENSP00000436113.1:p.Ala286Asp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.983C>A
  hgvsp: ENSP00000368874.3:p.Ala328Asp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.983C>A
  hgvsp: ENSP00000436194.1:p.Ala328Asp
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.425C>A
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26379
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4476
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3887
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala375Asp
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

11-15243190-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243190
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243190
    reference: chr 11
allele count: 6672
allele frequency: 5.782932029746737e-2
allele num: 115374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.861C>T
  hgvsp: ENST00000424273.1:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1128C>T
  hgvsp: ENST00000379554.3:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.987C>T
  hgvsp: ENST00000528567.1:c.987C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.987C>T
  hgvsp: ENST00000530161.1:c.987C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.429C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.861C>T
  hgvsp: ENST00000525218.1:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.987C>T
  hgvsp: ENST00000379556.3:c.987C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 533
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 369
genotype depth: GenotypeDepth
  all individuals: 9810
  bin: 2.25e1
  variant carriers: 462
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 3.75e1
  variant carriers: 839
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 1.75e1
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 7.5e0
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 25964
  bin: 2.75e1
  variant carriers: 575
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 1.25e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 4.25e1
  variant carriers: 880
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 684
genotype depth: GenotypeDepth
  all individuals: 10258
  bin: 3.25e1
  variant carriers: 777
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 95
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 6546
  bin: 6.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 1619
  bin: 7.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 7.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7579
  bin: 9.75e1
  variant carriers: 6188
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 8.25e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 3.75e1
  variant carriers: 9
hgvs: p.Leu376Leu
num of homozygotes: 311
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

11-15243191-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243191
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243191
    reference: chr 11
allele count: 7
allele frequency: 6.109268633269332e-5
allele num: 114580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.862G>A
  hgvsp: ENSP00000389161.1:p.Val288Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.862G>A
  hgvsp: ENSP00000436113.1:p.Val288Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.988G>A
  hgvsp: ENSP00000368874.3:p.Val330Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1129G>A
  hgvsp: ENSP00000368872.3:p.Val377Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.988G>A
  hgvsp: ENSP00000436194.1:p.Val330Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.988G>A
  hgvsp: ENSP00000435022.1:p.Val330Ile
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.430G>A
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28130
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5007
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7199
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37387
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val377Ile
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

11-15243191-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243191
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243191
    reference: chr 11
allele count: 2
allele frequency: 1.745505323791237e-5
allele num: 114580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.862G>T
  hgvsp: ENSP00000436113.1:p.Val288Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1129G>T
  hgvsp: ENSP00000368872.3:p.Val377Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.988G>T
  hgvsp: ENSP00000436194.1:p.Val330Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.988G>T
  hgvsp: ENSP00000435022.1:p.Val330Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.862G>T
  hgvsp: ENSP00000389161.1:p.Val288Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.988G>T
  hgvsp: ENSP00000368874.3:p.Val330Phe
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.430G>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1809
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val377Phe
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

11-15243213-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243213
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243213
    reference: chr 11
allele count: 1
allele frequency: 9.098684330245847e-6
allele num: 109906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.991+19C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1132+19C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.991+19C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.991+19C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.865+19C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.865+19C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.433+19C>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22347
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29774
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3032
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD

11-15243214-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243214
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243214
    reference: chr 11
allele count: 12
allele frequency: 1.09639104613979e-4
allele num: 109450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.865+20G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.991+20G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1132+20G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.865+20G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.433+20G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.991+20G>A
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.991+20G>A
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11452
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8712
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7018
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27413
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3638
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2859
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

11-15243224-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243224
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243224
    reference: chr 11
allele count: 1
allele frequency: 9.271793350269808e-6
allele num: 107854
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.865+30G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.991+30G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1132+30G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.433+30G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.991+30G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.865+30G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.991+30G>C
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15026
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1490
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3924
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20860
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4090
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

11-15243234-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243234
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243234
    reference: chr 11
allele count: 1
allele frequency: 9.527983688091925e-6
allele num: 104954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.865+40C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.991+40C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.991+40C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1132+40C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.991+40C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.433+40C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.865+40C>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6538
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4840
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10761
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7041
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8007
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

11-15243237-T-TTCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243237
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243240
    reference: chr 11
allele count: 1
allele frequency: 9.62982935942375e-6
allele num: 103844
alternate allele: TTCA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1132+43_1132+44insTCA
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.991+43_991+44insTCA
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.865+43_865+44insTCA
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.865+43_865+44insTCA
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.991+43_991+44insTCA
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.991+43_991+44insTCA
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.433+43_433+44insTCA
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8464
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1976
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1789
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3449
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4884
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10131
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

11-15243238-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15243238
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15243238
    reference: chr 11
allele count: 1
allele frequency: 9.642457669610831e-6
allele num: 103708
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.865+44G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.991+44G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.991+44G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1132+44G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.433+44G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.865+44G>C
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.991+44G>C
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16798
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4525
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3445
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1657
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7539
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4869
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10239
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

11-15247164-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15247164
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 15247164
    reference: chr 11
allele count: 70
allele frequency: 7.056167090036692e-4
allele num: 99204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436113
  ensembl transcript: ENST00000525218
  gene symbol: INSC
  hgvsc: ENST00000525218.1:c.866-32C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000435022
  ensembl transcript: ENST00000528567
  gene symbol: INSC
  hgvsc: ENST00000528567.1:c.992-32C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368872
  ensembl transcript: ENST00000379554
  gene symbol: INSC
  hgvsc: ENST00000379554.3:c.1133-32C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000368874
  ensembl transcript: ENST00000379556
  gene symbol: INSC
  hgvsc: ENST00000379556.3:c.992-32C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl transcript: ENST00000447214
  gene symbol: INSC
  hgvsc: ENST00000447214.2:n.434-32C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000389161
  ensembl transcript: ENST00000424273
  gene symbol: INSC
  hgvsc: ENST00000424273.1:c.866-32C>T
  variant of: http://identifiers.org/hgnc/33116
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188487
  ensembl protein: ENSP00000436194
  ensembl transcript: ENST00000530161
  gene symbol: INSC
  hgvsc: ENST00000530161.1:c.992-32C>T
  variant of: http://identifiers.org/hgnc/33116
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23507
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9937
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14337
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
num of homozygotes: 1
reference allele: C

GenotypeQuality
all individuals: 544
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1113
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2167
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.65892501658925e-4
allele num: 6028
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13106
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.219679064560268e-5
allele num: 48234
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 684
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.394700139470014e-4
allele num: 7170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4394
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.026252e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.047e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.324e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.03e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.39e-1

FS
type: SiteQuality
SIO_000300: 9.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.58e-1

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 307
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 6953
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2120
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 397
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 32892
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7626
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 861
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.896094046264695e-4
allele num: 5274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.018776791644026e-5
allele num: 33126
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2808
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.660989888238425e-4
allele num: 3758
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.155172413793103e-3
allele num: 464
num of homozygotes: 0

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

South Asian
type: Population
allele count: 254
allele frequency: 2.257777777777778e-2
allele num: 11250
num of homozygotes: 8

DP
type: SiteQuality
SIO_000300: 7.70204e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e0

VQSLOD
type: SiteQuality
SIO_000300: 5.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.562e1

GenotypeQuality
all individuals: 2562
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7119
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 829
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2127
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5070
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 5.757052389176742e-4
allele num: 3474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10860
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.74e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-1

DP
type: SiteQuality
SIO_000300: 7.45742e5

GenotypeQuality
all individuals: 2382
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2477
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5919
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27651
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2700
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.891196834817012e-5
allele num: 10110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2022
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.642e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.35e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

DP
type: SiteQuality
SIO_000300: 6.83725e5

QD
type: SiteQuality
SIO_000300: 1.479e1

FS
type: SiteQuality
SIO_000300: 2.434e0

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e0

GenotypeQuality
all individuals: 4735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2209
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3561
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 872
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23057
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9544
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1928
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1606
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.125e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.34227e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.307e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.76e-1

GenotypeQuality
all individuals: 2190
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3246
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3719
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4578
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 951
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.574983987556043e-5
allele num: 21858
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2026
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3936
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1570
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.06e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.29183e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

VQSLOD
type: SiteQuality
SIO_000300: -8.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

GenotypeQuality
all individuals: 2056
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 263
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4307
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1414
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

DP
type: SiteQuality
SIO_000300: 6.08712e5

VQSLOD
type: SiteQuality
SIO_000300: -1.671e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.25e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.81e0

GenotypeQuality
all individuals: 428
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12909
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6972
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2297
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2327
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6497
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8722
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16974
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1030
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1148
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1402
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.754e0

DP
type: SiteQuality
SIO_000300: 5.59854e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.78e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.366e0

QD
type: SiteQuality
SIO_000300: 8.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.754e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

GenotypeQuality
all individuals: 83
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9861
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 7.48e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.278e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.01e-2

DP
type: SiteQuality
SIO_000300: 5.56968e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

GenotypeQuality
all individuals: 1706
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14662
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1990
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
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: 1
allele frequency: 1.055966209081309e-4
allele num: 9470
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63554
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.382e1

MQRankSum
type: SiteQuality
SIO_000300: -1.334e0

VQSLOD
type: SiteQuality
SIO_000300: -9.88e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.309e0

FS
type: SiteQuality
SIO_000300: 1.104e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.09e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e-1

DP
type: SiteQuality
SIO_000300: 2.261959e6

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

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

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63586
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.055297593921486e-4
allele num: 9476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.366e0

QD
type: SiteQuality
SIO_000300: 1.006e1

FS
type: SiteQuality
SIO_000300: 2.79e0

VQSLOD
type: SiteQuality
SIO_000300: 7.67e-1

DP
type: SiteQuality
SIO_000300: 2.266722e6

MQRankSum
type: SiteQuality
SIO_000300: -7.5e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

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

GenotypeQuality
all individuals: 265
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 2.101281781886951e-4
allele num: 9518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10480
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

DP
type: SiteQuality
SIO_000300: 2.277044e6

MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
SIO_000300: 1.45e1

GenotypeQuality
all individuals: 44
bin: 5.25e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 5965
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64016
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.841620626151013e-4
allele num: 10860
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9544
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.412e1

FS
type: SiteQuality
SIO_000300: 4.447e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

DP
type: SiteQuality
SIO_000300: 2.283934e6

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26975
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14648
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1718
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64040
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: 8536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10934
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9546
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.643e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

VQSLOD
type: SiteQuality
SIO_000300: 4.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.468e0

DP
type: SiteQuality
SIO_000300: 2.284365e6

QD
type: SiteQuality
SIO_000300: 1.139e1

FS
type: SiteQuality
SIO_000300: 1.867e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 821
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GenotypeQuality
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variant carriers: 2

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: 1720
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variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.121585765568909e-5
allele num: 64070
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -3.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

QD
type: SiteQuality
SIO_000300: 1.365e1

DP
type: SiteQuality
SIO_000300: 2.285009e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.616e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 5993
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11280
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9568
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.81e0

MQRankSum
type: SiteQuality
SIO_000300: -3.44e-1

InbreedingCoeff
type: SiteQuality
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DP
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 1.205e1

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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11680
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.110516656816698e-5
allele num: 64298
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.54e-1

BaseQRankSum
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ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 2.29404e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.329518596840403e-5
allele num: 64312
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9580
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11724
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.984e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-1

FS
type: SiteQuality
SIO_000300: 1.812e0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12144
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551012811365822e-5
allele num: 64474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.934e1

DP
type: SiteQuality
SIO_000300: 2.299495e6

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

QD
type: SiteQuality
SIO_000300: 1.443e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

VQSLOD
type: SiteQuality
SIO_000300: 2.42e-1

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3339
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GenotypeQuality
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GenotypeQuality
all individuals: 822
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GenotypeQuality
all individuals: 279
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variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1733
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14644
bin: 9.75e1
variant carriers: 1

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549522746993926e-5
allele num: 64536
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.300958e6

FS
type: SiteQuality
SIO_000300: 2.971e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.33e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.58e0

MQRankSum
type: SiteQuality
SIO_000300: -1.68e-1

QD
type: SiteQuality
SIO_000300: 1.209e1

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14639
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6034
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 28063
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.54640769492469e-5
allele num: 64666
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.945336087716511e-5
allele num: 12586
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.7e-1

DP
type: SiteQuality
SIO_000300: 2.307148e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.224e1

GenotypeQuality
all individuals: 490
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6077
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28404
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14644
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 2016
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.038421599169263e-4
allele num: 9630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.71390663087414e-5
allele num: 64818
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 9.267840593141798e-4
allele num: 12948
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.09e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

DP
type: SiteQuality
SIO_000300: 2.311304e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2052
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14628
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 287
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1310
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531909678605349e-5
allele num: 65278
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.333506673600277e-4
allele num: 11538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14370
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.59e-1

FS
type: SiteQuality
SIO_000300: 3.302e0

DP
type: SiteQuality
SIO_000300: 2.329513e6

QD
type: SiteQuality
SIO_000300: 1.047e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

GenotypeQuality
all individuals: 1833
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1766
bin: 7.25e1
variant carriers: 4

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

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 185
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 359
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6136
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 255
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 2

South Asian
type: Population
allele count: 445
allele frequency: 3.031748194576918e-2
allele num: 14678
num of homozygotes: 9

Latino
type: Population
allele count: 167
allele frequency: 1.446638946638947e-2
allele num: 11544
num of homozygotes: 2

African
type: Population
allele count: 72
allele frequency: 7.434944237918215e-3
allele num: 9684
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2572
allele frequency: 3.932721712538226e-2
allele num: 65400
num of homozygotes: 59

Other
type: Population
allele count: 19
allele frequency: 2.188940092165899e-2
allele num: 868
num of homozygotes: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 158
allele frequency: 2.392489400363416e-2
allele num: 6604
num of homozygotes: 4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.33e0

DP
type: SiteQuality
SIO_000300: 2.41151e6

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

QD
type: SiteQuality
SIO_000300: 1.319e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.51e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12313
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1367
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6575
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1726
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 9.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.018e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 2.200727e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1880
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31489
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6616
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2184
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15214
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164415463437354e-4
allele num: 8588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.947e1

DP
type: SiteQuality
SIO_000300: 2.205941e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

MQRankSum
type: SiteQuality
SIO_000300: 9.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.949e0

VQSLOD
type: SiteQuality
SIO_000300: 3.24e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

GenotypeQuality
all individuals: 2183
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12312
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 635
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 246
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.028467595396729e-4
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9698
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65742
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.208351e6

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.73e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.442e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

QD
type: SiteQuality
SIO_000300: 1.17e0

GenotypeQuality
all individuals: 154
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31602
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65708
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15602
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.097893432465923e-4
allele num: 9684
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.09e1

DP
type: SiteQuality
SIO_000300: 2.211281e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.07e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.687e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

GenotypeQuality
all individuals: 106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 6465
bin: 6.75e1
variant carriers: 12

GenotypeQuality
all individuals: 149
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 244
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1805
bin: 7.25e1
variant carriers: 9

GenotypeQuality
all individuals: 13735
bin: 9.75e1
variant carriers: 7713

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 5886
allele frequency: 8.936053926033886e-2
allele num: 65868
num of homozygotes: 267

African
type: Population
allele count: 135
allele frequency: 1.393476465730801e-2
allele num: 9688
num of homozygotes: 1

South Asian
type: Population
allele count: 1120
allele frequency: 7.08502024291498e-2
allele num: 15808
num of homozygotes: 42

Latino
type: Population
allele count: 492
allele frequency: 4.257528556593977e-2
allele num: 11556
num of homozygotes: 18

East Asian
type: Population
allele count: 5
allele frequency: 5.824790307548928e-4
allele num: 8584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 419
allele frequency: 6.385248399878087e-2
allele num: 6562
num of homozygotes: 13

Other
type: Population
allele count: 74
allele frequency: 8.409090909090909e-2
allele num: 880
num of homozygotes: 6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.09e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 2.341922e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.46e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

QD
type: SiteQuality
SIO_000300: 1.311e1

FS
type: SiteQuality
SIO_000300: 5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e0

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

GenotypeQuality
all individuals: 163
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 133
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36029
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6663
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15914
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.038774766014343e-5
allele num: 65816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

DP
type: SiteQuality
SIO_000300: 1.894892e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.331e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

QD
type: SiteQuality
SIO_000300: 1.59e0

VQSLOD
type: SiteQuality
SIO_000300: -1.532e0

GenotypeQuality
all individuals: 167
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 543
bin: 8.75e1
variant carriers: 10

GenotypeQuality
all individuals: 256
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 175
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7265
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 131
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1278
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2141
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 696
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 4657
bin: 9.75e1
variant carriers: 82

European (Finnish)
type: Population
allele count: 33
allele frequency: 6.235827664399093e-3
allele num: 5292
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.638986629134412e-4
allele num: 11368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15966
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 88
allele frequency: 1.42847867021622e-3
allele num: 61604
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.512683267395858e-3
allele num: 8594
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.755111745126011e-4
allele num: 8412
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.455e2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.58e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.26464e2

QD
type: SiteQuality
SIO_000300: 1.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.776e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.066e0

DP
type: SiteQuality
SIO_000300: 1.9207e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.75e-2

MQ
type: SiteQuality
SIO_000300: 5.89e1

GenotypeQuality
all individuals: 722
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38706
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2386
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 762
bin: 9.25e1
variant carriers: 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: 9710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66132
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.13195977434388e-5
allele num: 16308
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

FS
type: SiteQuality
SIO_000300: 9.15e-1

QD
type: SiteQuality
SIO_000300: 1.25e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 1.807351e6

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 4.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4897
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8021
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66138
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 2.66e0

DP
type: SiteQuality
SIO_000300: 1.807626e6

VQSLOD
type: SiteQuality
SIO_000300: -2.532e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.76e-1

FS
type: SiteQuality
SIO_000300: 4.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1423
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8013
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2379
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4898
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 156
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66134
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.030290541932825e-4
allele num: 9706
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: 8584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.55e-1

QD
type: SiteQuality
SIO_000300: 1.388e1

MQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

DP
type: SiteQuality
SIO_000300: 1.807682e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.76e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

FS
type: SiteQuality
SIO_000300: 2.378e0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

GenotypeQuality
all individuals: 179
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2379
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38804
bin: 6.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 4892
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 1424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8032
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.030078285949732e-4
allele num: 9708
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 9.154155986818016e-4
allele num: 16386
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66110
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

DP
type: SiteQuality
SIO_000300: 1.807609e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.636e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.325e1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

FS
type: SiteQuality
SIO_000300: 1.129e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

GenotypeQuality
all individuals: 8019
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 592
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4878
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 758
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38761
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-5
allele num: 66080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.714e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.563e-1

FS
type: SiteQuality
SIO_000300: 3.355e0

QD
type: SiteQuality
SIO_000300: 1.046e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.353e0

DP
type: SiteQuality
SIO_000300: 1.806471e6

GenotypeQuality
all individuals: 2139
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38779
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8024
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 8.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66078
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.094588005850804e-5
allele num: 16408
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.79e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 2.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 1.806183e6

QD
type: SiteQuality
SIO_000300: 1.105e1

MQRankSum
type: SiteQuality
SIO_000300: -9.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8010
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2135
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.217878455730118e-4
allele num: 16422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.54063871651279e-5
allele num: 66070
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.665267086540705e-4
allele num: 8574
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.032204789430223e-4
allele num: 9688
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQ
type: SiteQuality
SIO_000300: 5.94e1

QD
type: SiteQuality
SIO_000300: 1.235e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: -2.34e-1

FS
type: SiteQuality
SIO_000300: 3.451e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 1.80602e6

GenotypeQuality
all individuals: 151
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4876
bin: 9.75e1
variant carriers: 112

GenotypeQuality
all individuals: 2136
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 11
allele frequency: 6.693440428380187e-4
allele num: 16434
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.06654267410622e-4
allele num: 9678
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.028192471913515e-5
allele num: 66046
num of homozygotes: 0

East Asian
type: Population
allele count: 96
allele frequency: 1.119402985074627e-2
allele num: 8576
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.126126126126126e-3
allele num: 888
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.805362e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

QD
type: SiteQuality
SIO_000300: 1.44e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

FS
type: SiteQuality
SIO_000300: 1.179e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

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

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38879
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2143
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 755
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.516530178950561e-4
allele num: 6594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66048
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.599e0

QD
type: SiteQuality
SIO_000300: 1.191e1

DP
type: SiteQuality
SIO_000300: 1.799741e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

FS
type: SiteQuality
SIO_000300: 2.135e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.56e-1

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

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

GenotypeQuality
all individuals: 710
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2370
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2133
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514050387596899e-5
allele num: 66048
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.7e-1

DP
type: SiteQuality
SIO_000300: 1.797467e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 7.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.13e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.743e1

GenotypeQuality
all individuals: 180
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2363
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39051
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7993
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4747
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514646632940535e-5
allele num: 66022
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.244e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

DP
type: SiteQuality
SIO_000300: 1.796556e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.012e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 3.152e0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

VQSLOD
type: SiteQuality
SIO_000300: 3.43e-1

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

GenotypeQuality
all individuals: 38945
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7990
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4746
bin: 9.75e1
variant carriers: 6

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9680
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.091184581350951e-5
allele num: 65998
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.183e0

VQSLOD
type: SiteQuality
SIO_000300: -1.112e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.795134e6

MQ
type: SiteQuality
SIO_000300: 5.547e1

QD
type: SiteQuality
SIO_000300: 1.317e1

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2110
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2345
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1396
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7930
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.097801364670205e-5
allele num: 65950
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 1.793899e6

MQ
type: SiteQuality
SIO_000300: 5.538e1

MQRankSum
type: SiteQuality
SIO_000300: -1.479e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.613e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 1.737e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 168
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7945
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4736
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 744
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1396
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9664
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.094767477111502e-5
allele num: 65972
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.48e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.98e-1

DP
type: SiteQuality
SIO_000300: 1.793901e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

MQRankSum
type: SiteQuality
SIO_000300: -1.721e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 1.753e1

VQSLOD
type: SiteQuality
SIO_000300: -8.761e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 579
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4731
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1395
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2116
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65976
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.034554107179805e-4
allele num: 9666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

DP
type: SiteQuality
SIO_000300: 1.793825e6

FS
type: SiteQuality
SIO_000300: 5.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.567e0

VQSLOD
type: SiteQuality
SIO_000300: 5.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 1.18e1

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

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

GenotypeQuality
all individuals: 7924
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38783
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2109
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

African
type: Population
allele count: 8
allele frequency: 8.300477277443454e-4
allele num: 9638
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65946
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.601e0

DP
type: SiteQuality
SIO_000300: 1.792462e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 3.584e0

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

QD
type: SiteQuality
SIO_000300: 1.164e1

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38894
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2336
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4717
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2107
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1394
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7928
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.330504070673827e-4
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65946
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
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: 0
allele frequency: 0.0e0
allele num: 9640
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.619e0

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.86e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.088e0

QD
type: SiteQuality
SIO_000300: 1.164e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.31e-1

DP
type: SiteQuality
SIO_000300: 1.791566e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

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

GenotypeQuality
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bin: 7.5e0
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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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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 2334
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GenotypeQuality
all individuals: 38948
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.081245439065921e-5
allele num: 16444
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65940
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.791169e6

VQSLOD
type: SiteQuality
SIO_000300: -7.254e-1

FS
type: SiteQuality
SIO_000300: 6.474e0

QD
type: SiteQuality
SIO_000300: 1.247e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.345e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

GenotypeQuality
all individuals: 967
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16767865483419e-4
allele num: 8564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.038637307852098e-4
allele num: 9628
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.789648e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.84e-1

FS
type: SiteQuality
SIO_000300: 4.42e-1

QD
type: SiteQuality
SIO_000300: 1.299e1

MQ
type: SiteQuality
SIO_000300: 5.901e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.25e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.217e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.76e-1

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 150
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.553319369820599e-5
allele num: 65886
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16767865483419e-4
allele num: 8564
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

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

South Asian
type: Population
allele count: 6
allele frequency: 3.650967506389193e-4
allele num: 16434
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

MQ
type: SiteQuality
SIO_000300: 5.989e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.17e0

DP
type: SiteQuality
SIO_000300: 1.789616e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

QD
type: SiteQuality
SIO_000300: 1.25e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-2

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2254
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variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.572752492150108e-5
allele num: 65606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.223e1

FS
type: SiteQuality
SIO_000300: 1.859e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.045e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.776e0

VQSLOD
type: SiteQuality
SIO_000300: 3.0e0

DP
type: SiteQuality
SIO_000300: 1.775875e6

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
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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: 26
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variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65366
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9548
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.338634237605239e-4
allele num: 8552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16050
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.462e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

FS
type: SiteQuality
SIO_000300: 6.45e-1

DP
type: SiteQuality
SIO_000300: 1.765382e6

QD
type: SiteQuality
SIO_000300: 7.3e0

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.093e-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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bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15974
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East Asian
type: Population
allele count: 1
allele frequency: 1.169043722235212e-4
allele num: 8554
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.183e1

FS
type: SiteQuality
SIO_000300: 4.355e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-1

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

DP
type: SiteQuality
SIO_000300: 1.761368e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-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
all individuals: 89
bin: 5.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.507951356407858e-4
allele num: 8552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64982
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.933e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.743267e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 15584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64952
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
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African
type: Population
allele count: 1
allele frequency: 1.056189269117026e-4
allele num: 9468
num of homozygotes: 0

Other
type: Population
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allele num: 868
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.82e0

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 267
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.170686022008897e-4
allele num: 8542
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.462453147214683e-5
allele num: 15474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9430
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64840
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.504e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.182e0

QD
type: SiteQuality
SIO_000300: 1.129e1

VQSLOD
type: SiteQuality
SIO_000300: 5.1e-1

DP
type: SiteQuality
SIO_000300: 1.736874e6

MQRankSum
type: SiteQuality
SIO_000300: 4.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

GenotypeQuality
all individuals: 3100
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2137
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36225
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1911
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

Other
type: Population
allele count: 8
allele frequency: 9.237875288683603e-3
allele num: 866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 191
allele frequency: 2.96952736318408e-2
allele num: 6432
num of homozygotes: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9436
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.45577792123951e-5
allele num: 15490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 73
allele frequency: 1.126299873484124e-3
allele num: 64814
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.074e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.12e0

QD
type: SiteQuality
SIO_000300: 1.326e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 1.735668e6

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

GenotypeQuality
all individuals: 3521
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4487
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 7246
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2129
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1291
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.68384074941452e-4
allele num: 8540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15266
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9352
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.610000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.983e0

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

DP
type: SiteQuality
SIO_000300: 1.717886e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.15e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

GenotypeQuality
all individuals: 1295
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35493
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7246
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3542
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64554
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 1.717394e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 1.305e1

MQRankSum
type: SiteQuality
SIO_000300: 8.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.39e-1

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

GenotypeQuality
all individuals: 354
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1288
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7038
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.553277415346381e-5
allele num: 64380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.577e0

FS
type: SiteQuality
SIO_000300: 1.3797e1

QD
type: SiteQuality
SIO_000300: 1.185e1

VQSLOD
type: SiteQuality
SIO_000300: -1.889e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.707819e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

GenotypeQuality
all individuals: 138
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6984
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2068
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35060
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1834
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.661698163428267e-4
allele num: 15028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.887e0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.353e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

DP
type: SiteQuality
SIO_000300: 1.70682e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.053e1

GenotypeQuality
all individuals: 191
bin: 4.75e1
variant carriers: 7

GenotypeQuality
all individuals: 4214
bin: 2.25e1
variant carriers: 8

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 34052
bin: 6.25e1
variant carriers: 20

GenotypeQuality
all individuals: 729
bin: 3.25e1
variant carriers: 8

GenotypeQuality
all individuals: 182
bin: 4.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1675
bin: 7.75e1
variant carriers: 19

GenotypeQuality
all individuals: 225
bin: 5.75e1
variant carriers: 17

GenotypeQuality
all individuals: 300
bin: 9.25e1
variant carriers: 31

GenotypeQuality
all individuals: 301
bin: 8.75e1
variant carriers: 21

Latino
type: Population
allele count: 534
allele frequency: 4.677645409950946e-2
allele num: 11416
num of homozygotes: 14

African
type: Population
allele count: 1741
allele frequency: 1.874461670973299e-1
allele num: 9288
num of homozygotes: 176

European (Non-Finnish)
type: Population
allele count: 2698
allele frequency: 4.209573737751982e-2
allele num: 64092
num of homozygotes: 56

South Asian
type: Population
allele count: 832
allele frequency: 5.594405594405594e-2
allele num: 14872
num of homozygotes: 36

East Asian
type: Population
allele count: 550
allele frequency: 6.450856204550785e-2
allele num: 8526
num of homozygotes: 19

European (Finnish)
type: Population
allele count: 265
allele frequency: 4.182449494949495e-2
allele num: 6336
num of homozygotes: 7

Other
type: Population
allele count: 52
allele frequency: 6.161137440758294e-2
allele num: 844
num of homozygotes: 3

QD
type: SiteQuality
SIO_000300: 1.408e1

FS
type: SiteQuality
SIO_000300: 6.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

DP
type: SiteQuality
SIO_000300: 1.698253e6

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.08e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.83e0

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 476
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1809
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1748
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14606
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.571741511500548e-4
allele num: 9130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567005139776858e-5
allele num: 63816
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.197e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.12e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 5.85e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.231e1

DP
type: SiteQuality
SIO_000300: 1.581766e6

GenotypeQuality
all individuals: 305
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7199
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5007
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37387
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 293
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1592
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.846501437765302e-5
allele num: 14606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567005139776858e-5
allele num: 63816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6290
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 9.12e-1

FS
type: SiteQuality
SIO_000300: 5.85e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.197e0

DP
type: SiteQuality
SIO_000300: 1.581766e6

MQRankSum
type: SiteQuality
SIO_000300: -3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.28e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

GenotypeQuality
all individuals: 1576
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2438
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9260
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5291
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6072
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.621323648626739e-5
allele num: 61678
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13280
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: 4.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

FS
type: SiteQuality
SIO_000300: 2.978e0

DP
type: SiteQuality
SIO_000300: 1.411333e6

MQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.243e1

GenotypeQuality
all individuals: 756
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1547
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9831
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4736
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6056
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.254996419503939e-5
allele num: 61444
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.166044776119403e-3
allele num: 8576
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.598e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

DP
type: SiteQuality
SIO_000300: 1.37598e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.62e-1

FS
type: SiteQuality
SIO_000300: 1.606e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 534
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3809
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5955
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11305
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.177578897786152e-4
allele num: 8492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10972
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5966
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12660
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.004e1

VQSLOD
type: SiteQuality
SIO_000300: 9.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

FS
type: SiteQuality
SIO_000300: 3.732e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.208e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

DP
type: SiteQuality
SIO_000300: 1.258543e6

MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeQuality
all individuals: 3264
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2893
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10876
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1052
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5812
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.267840593141798e-5
allele num: 10790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11794
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59514
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.373e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.137e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.803e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 1.13288e6

QD
type: SiteQuality
SIO_000300: 1.698e1

GenotypeQuality
all individuals: 7823
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 585
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4538
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7548
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8196
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10680
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59050
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.224289911851126e-4
allele num: 8168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.936e0

QD
type: SiteQuality
SIO_000300: 1.708e1

DP
type: SiteQuality
SIO_000300: 1.105639e6

MQRankSum
type: SiteQuality
SIO_000300: -2.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

MQ
type: SiteQuality
SIO_000300: 5.237e1

GenotypeQuality
all individuals: 8176
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2286
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8250
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 317
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10680
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7934
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.228199459592238e-4
allele num: 8142
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5770
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.167e0

DP
type: SiteQuality
SIO_000300: 1.104582e6

VQSLOD
type: SiteQuality
SIO_000300: -1.669e0

QD
type: SiteQuality
SIO_000300: 1.63e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.955e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.051e0

MQ
type: SiteQuality
SIO_000300: 5.329e1