10-24813295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813295
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813295
    reference: chr 10
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1549G>A
  hgvsp: ENSP00000302343.6:p.Ala517Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2395G>A
  hgvsp: ENSP00000365635.3:p.Ala799Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2260G>A
  hgvsp: ENSP00000365645.1:p.Ala754Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1549G>A
  hgvsp: ENSP00000365634.2:p.Ala517Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2395G>A
  hgvsp: ENSP00000392625.1:p.Ala799Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1945G>A
  hgvsp: ENSP00000404798.1:p.Ala649Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1549G>A
  hgvsp: ENSP00000379722.1:p.Ala517Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2395G>A
  hgvsp: ENSP00000365639.4:p.Ala799Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2500G>A
  hgvsp: ENSP00000365637.3:p.Ala834Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1549G>A
  hgvsp: ENSP00000379723.1:p.Ala517Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3570G>A
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala834Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

10-24813297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813297
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813297
    reference: chr 10
allele count: 230
allele frequency: 1.897220160026396e-3
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1551C>T
  hgvsp: ENST00000376451.2:c.1551C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1551C>T
  hgvsp: ENST00000396446.1:c.1551C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2397C>T
  hgvsp: ENST00000376452.3:c.2397C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2502C>T
  hgvsp: ENST00000376454.3:c.2502C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1947C>T
  hgvsp: ENST00000438429.1:c.1947C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1551C>T
  hgvsp: ENST00000307544.6:c.1551C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2397C>T
  hgvsp: ENST00000458595.1:c.2397C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3568C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2397C>T
  hgvsp: ENST00000376456.4:c.2397C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2262C>T
  hgvsp: ENST00000376462.1:c.2262C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1551C>T
  hgvsp: ENST00000396445.1:c.1551C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8711
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 15723
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 4.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 6.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 8057
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 9.75e1
  variant carriers: 46
genotype quality: GenotypeQuality
hgvs: p.Ala834Ala
num of homozygotes: 3
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

10-24813298-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813298
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813298
    reference: chr 10
allele count: 19
allele frequency: 1.567191263321126e-4
allele num: 121236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3567G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1552G>A
  hgvsp: ENSP00000365634.2:p.Ala518Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2398G>A
  hgvsp: ENSP00000365635.3:p.Ala800Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2263G>A
  hgvsp: ENSP00000365645.1:p.Ala755Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1552G>A
  hgvsp: ENSP00000379723.1:p.Ala518Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1552G>A
  hgvsp: ENSP00000379722.1:p.Ala518Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2503G>A
  hgvsp: ENSP00000365637.3:p.Ala835Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2398G>A
  hgvsp: ENSP00000392625.1:p.Ala800Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1552G>A
  hgvsp: ENSP00000302343.6:p.Ala518Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1948G>A
  hgvsp: ENSP00000404798.1:p.Ala650Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2398G>A
  hgvsp: ENSP00000365639.4:p.Ala800Thr
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala835Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

10-24813308-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813308
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813308
    reference: chr 10
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2408T>C
  hgvsp: ENSP00000365639.4:p.Met803Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1958T>C
  hgvsp: ENSP00000404798.1:p.Met653Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3557T>C
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2408T>C
  hgvsp: ENSP00000392625.1:p.Met803Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1562T>C
  hgvsp: ENSP00000379723.1:p.Met521Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2513T>C
  hgvsp: ENSP00000365637.3:p.Met838Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1562T>C
  hgvsp: ENSP00000379722.1:p.Met521Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1562T>C
  hgvsp: ENSP00000302343.6:p.Met521Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2273T>C
  hgvsp: ENSP00000365645.1:p.Met758Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2408T>C
  hgvsp: ENSP00000365635.3:p.Met803Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1562T>C
  hgvsp: ENSP00000365634.2:p.Met521Thr
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met838Thr
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

10-24813313-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813313
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813313
    reference: chr 10
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1567A>G
  hgvsp: ENSP00000379723.1:p.Met523Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2278A>G
  hgvsp: ENSP00000365645.1:p.Met760Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3552A>G
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1963A>G
  hgvsp: ENSP00000404798.1:p.Met655Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2413A>G
  hgvsp: ENSP00000392625.1:p.Met805Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2518A>G
  hgvsp: ENSP00000365637.3:p.Met840Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1567A>G
  hgvsp: ENSP00000379722.1:p.Met523Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1567A>G
  hgvsp: ENSP00000302343.6:p.Met523Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1567A>G
  hgvsp: ENSP00000365634.2:p.Met523Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2413A>G
  hgvsp: ENSP00000365639.4:p.Met805Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2413A>G
  hgvsp: ENSP00000365635.3:p.Met805Val
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met840Val
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

10-24813313-ATGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813313
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813310
    reference: chr 10
allele count: 84
allele frequency: 6.927149477989807e-4
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2414_2416delTGG
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1568_1570delTGG
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2279_2281delTGG
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1568_1570delTGG
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2414_2416delTGG
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2414_2416delTGG
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1964_1966delTGG
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3551_*-3549delTGG
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2519_2521delTGG
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1568_1570delTGG
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1568_1570delTGG
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 15775
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met840_Glu841delinsLys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: ATGG
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

10-24813314-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813314
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813314
    reference: chr 10
allele count: 2
allele frequency: 1.651718613217052e-5
allele num: 121086
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2519T>C
  hgvsp: ENSP00000365637.3:p.Met840Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1568T>C
  hgvsp: ENSP00000365634.2:p.Met523Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2414T>C
  hgvsp: ENSP00000365639.4:p.Met805Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1568T>C
  hgvsp: ENSP00000379722.1:p.Met523Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2414T>C
  hgvsp: ENSP00000392625.1:p.Met805Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2279T>C
  hgvsp: ENSP00000365645.1:p.Met760Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1964T>C
  hgvsp: ENSP00000404798.1:p.Met655Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1568T>C
  hgvsp: ENSP00000379723.1:p.Met523Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2414T>C
  hgvsp: ENSP00000365635.3:p.Met805Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3551T>C
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1568T>C
  hgvsp: ENSP00000302343.6:p.Met523Thr
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met840Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

10-24813319-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813319
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813319
    reference: chr 10
allele count: 109
allele frequency: 8.98820813061763e-4
allele num: 121270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2419A>G
  hgvsp: ENSP00000392625.1:p.Lys807Glu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1969A>G
  hgvsp: ENSP00000404798.1:p.Lys657Glu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2524A>G
  hgvsp: ENSP00000365637.3:p.Lys842Glu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2284A>G
  hgvsp: ENSP00000365645.1:p.Lys762Glu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1573A>G
  hgvsp: ENSP00000379723.1:p.Lys525Glu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1573A>G
  hgvsp: ENSP00000302343.6:p.Lys525Glu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2419A>G
  hgvsp: ENSP00000365639.4:p.Lys807Glu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1573A>G
  hgvsp: ENSP00000379722.1:p.Lys525Glu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1573A>G
  hgvsp: ENSP00000365634.2:p.Lys525Glu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3546A>G
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2419A>G
  hgvsp: ENSP00000365635.3:p.Lys807Glu
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8098
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 15762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Lys842Glu
num of homozygotes: 2
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-24813322-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813322
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813322
    reference: chr 10
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2527G>C
  hgvsp: ENSP00000365637.3:p.Ala843Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1972G>C
  hgvsp: ENSP00000404798.1:p.Ala658Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1576G>C
  hgvsp: ENSP00000302343.6:p.Ala526Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2422G>C
  hgvsp: ENSP00000365635.3:p.Ala808Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2422G>C
  hgvsp: ENSP00000392625.1:p.Ala808Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1576G>C
  hgvsp: ENSP00000365634.2:p.Ala526Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2422G>C
  hgvsp: ENSP00000365639.4:p.Ala808Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1576G>C
  hgvsp: ENSP00000379723.1:p.Ala526Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2287G>C
  hgvsp: ENSP00000365645.1:p.Ala763Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1576G>C
  hgvsp: ENSP00000379722.1:p.Ala526Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3543G>C
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala843Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/10-24813325-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813325
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813325
    reference: chr 10
allele count: 4
allele frequency: 3.301855642871293e-5
allele num: 121144
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2425A>C
  hgvsp: ENSP00000365635.3:p.Thr809Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2425A>C
  hgvsp: ENSP00000365639.4:p.Thr809Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1579A>C
  hgvsp: ENSP00000302343.6:p.Thr527Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2425A>C
  hgvsp: ENSP00000392625.1:p.Thr809Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1579A>C
  hgvsp: ENSP00000379723.1:p.Thr527Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2290A>C
  hgvsp: ENSP00000365645.1:p.Thr764Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3540A>C
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1579A>C
  hgvsp: ENSP00000379722.1:p.Thr527Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2530A>C
  hgvsp: ENSP00000365637.3:p.Thr844Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1579A>C
  hgvsp: ENSP00000365634.2:p.Thr527Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1975A>C
  hgvsp: ENSP00000404798.1:p.Thr659Pro
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8117
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr844Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

10-24813325-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813325
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813325
    reference: chr 10
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2290A>G
  hgvsp: ENSP00000365645.1:p.Thr764Ala
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2425A>G
  hgvsp: ENSP00000365639.4:p.Thr809Ala
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1579A>G
  hgvsp: ENSP00000379722.1:p.Thr527Ala
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1579A>G
  hgvsp: ENSP00000365634.2:p.Thr527Ala
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1579A>G
  hgvsp: ENSP00000379723.1:p.Thr527Ala
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1579A>G
  hgvsp: ENSP00000302343.6:p.Thr527Ala
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1975A>G
  hgvsp: ENSP00000404798.1:p.Thr659Ala
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2425A>G
  hgvsp: ENSP00000365635.3:p.Thr809Ala
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3540A>G
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2425A>G
  hgvsp: ENSP00000392625.1:p.Thr809Ala
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2530A>G
  hgvsp: ENSP00000365637.3:p.Thr844Ala
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr844Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-24813326-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813326
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813326
    reference: chr 10
allele count: 2
allele frequency: 1.649266900862567e-5
allele num: 121266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2291C>T
  hgvsp: ENSP00000365645.1:p.Thr764Ile
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1580C>T
  hgvsp: ENSP00000379722.1:p.Thr527Ile
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2426C>T
  hgvsp: ENSP00000392625.1:p.Thr809Ile
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1580C>T
  hgvsp: ENSP00000302343.6:p.Thr527Ile
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2426C>T
  hgvsp: ENSP00000365639.4:p.Thr809Ile
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1976C>T
  hgvsp: ENSP00000404798.1:p.Thr659Ile
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2426C>T
  hgvsp: ENSP00000365635.3:p.Thr809Ile
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2531C>T
  hgvsp: ENSP00000365637.3:p.Thr844Ile
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1580C>T
  hgvsp: ENSP00000379723.1:p.Thr527Ile
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1580C>T
  hgvsp: ENSP00000365634.2:p.Thr527Ile
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3539C>T
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr844Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

10-24813327-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813327
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813327
    reference: chr 10
allele count: 10080
allele frequency: 8.31353919239905e-2
allele num: 121248
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2532A>G
  hgvsp: ENST00000376454.3:c.2532A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1581A>G
  hgvsp: ENST00000307544.6:c.1581A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1581A>G
  hgvsp: ENST00000376451.2:c.1581A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2292A>G
  hgvsp: ENST00000376462.1:c.2292A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1581A>G
  hgvsp: ENST00000396446.1:c.1581A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2427A>G
  hgvsp: ENST00000458595.1:c.2427A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1581A>G
  hgvsp: ENST00000396445.1:c.1581A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2427A>G
  hgvsp: ENST00000376452.3:c.2427A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1977A>G
  hgvsp: ENST00000438429.1:c.1977A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2427A>G
  hgvsp: ENST00000376456.4:c.2427A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3538A>G
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15697
  bin: 2.75e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 4.25e1
  variant carriers: 568
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8531
  bin: 2.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 6.75e1
  variant carriers: 818
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 8.75e1
  variant carriers: 358
genotype depth: GenotypeDepth
  all individuals: 7940
  bin: 3.25e1
  variant carriers: 250
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 493
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.75e1
  variant carriers: 1075
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 6.25e1
  variant carriers: 943
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 5.75e1
  variant carriers: 937
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 5.25e1
  variant carriers: 888
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.25e1
  variant carriers: 741
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.75e1
  variant carriers: 760
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 311
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 577
genotype quality: GenotypeQuality
hgvs: p.Thr844Thr
num of homozygotes: 719
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

10-24813331-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813331
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813331
    reference: chr 10
allele count: 5
allele frequency: 4.123439278233189e-5
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1585G>A
  hgvsp: ENSP00000302343.6:p.Ala529Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2431G>A
  hgvsp: ENSP00000365635.3:p.Ala811Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2296G>A
  hgvsp: ENSP00000365645.1:p.Ala766Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1585G>A
  hgvsp: ENSP00000365634.2:p.Ala529Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2431G>A
  hgvsp: ENSP00000365639.4:p.Ala811Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1585G>A
  hgvsp: ENSP00000379722.1:p.Ala529Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3534G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1981G>A
  hgvsp: ENSP00000404798.1:p.Ala661Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1585G>A
  hgvsp: ENSP00000379723.1:p.Ala529Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2431G>A
  hgvsp: ENSP00000392625.1:p.Ala811Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2536G>A
  hgvsp: ENSP00000365637.3:p.Ala846Thr
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala846Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-24813342-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813342
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813342
    reference: chr 10
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1596G>T
  hgvsp: ENST00000396445.1:c.1596G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2442G>T
  hgvsp: ENST00000458595.1:c.2442G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1992G>T
  hgvsp: ENST00000438429.1:c.1992G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1596G>T
  hgvsp: ENST00000307544.6:c.1596G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2547G>T
  hgvsp: ENST00000376454.3:c.2547G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1596G>T
  hgvsp: ENST00000376451.2:c.1596G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2442G>T
  hgvsp: ENST00000376456.4:c.2442G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2442G>T
  hgvsp: ENST00000376452.3:c.2442G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3523G>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1596G>T
  hgvsp: ENST00000396446.1:c.1596G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2307G>T
  hgvsp: ENST00000376462.1:c.2307G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu849Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

10-24813347-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813347
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813347
    reference: chr 10
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2312G>A
  hgvsp: ENSP00000365645.1:p.Ser771Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.1997G>A
  hgvsp: ENSP00000404798.1:p.Ser666Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3518G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2552G>A
  hgvsp: ENSP00000365637.3:p.Ser851Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2447G>A
  hgvsp: ENSP00000365639.4:p.Ser816Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2447G>A
  hgvsp: ENSP00000392625.1:p.Ser816Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1601G>A
  hgvsp: ENSP00000379722.1:p.Ser534Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2447G>A
  hgvsp: ENSP00000365635.3:p.Ser816Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1601G>A
  hgvsp: ENSP00000379723.1:p.Ser534Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1601G>A
  hgvsp: ENSP00000302343.6:p.Ser534Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1601G>A
  hgvsp: ENSP00000365634.2:p.Ser534Asn
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser851Asn
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

10-24813352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813352
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813352
    reference: chr 10
allele count: 7
allele frequency: 5.774148313123814e-5
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1606G>A
  hgvsp: ENSP00000379723.1:p.Glu536Lys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1606G>A
  hgvsp: ENSP00000365634.2:p.Glu536Lys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2002G>A
  hgvsp: ENSP00000404798.1:p.Glu668Lys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2452G>A
  hgvsp: ENSP00000365635.3:p.Glu818Lys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2452G>A
  hgvsp: ENSP00000365639.4:p.Glu818Lys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1606G>A
  hgvsp: ENSP00000302343.6:p.Glu536Lys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2557G>A
  hgvsp: ENSP00000365637.3:p.Glu853Lys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3513G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2452G>A
  hgvsp: ENSP00000392625.1:p.Glu818Lys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2317G>A
  hgvsp: ENSP00000365645.1:p.Glu773Lys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1606G>A
  hgvsp: ENSP00000379722.1:p.Glu536Lys
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu853Lys
num of homozygotes: 1
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

10-24813363-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813363
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813363
    reference: chr 10
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1617C>T
  hgvsp: ENST00000396445.1:c.1617C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2463C>T
  hgvsp: ENST00000376452.3:c.2463C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3502C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1617C>T
  hgvsp: ENST00000307544.6:c.1617C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1617C>T
  hgvsp: ENST00000376451.2:c.1617C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2463C>T
  hgvsp: ENST00000458595.1:c.2463C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2568C>T
  hgvsp: ENST00000376454.3:c.2568C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1617C>T
  hgvsp: ENST00000396446.1:c.1617C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2328C>T
  hgvsp: ENST00000376462.1:c.2328C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2013C>T
  hgvsp: ENST00000438429.1:c.2013C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2463C>T
  hgvsp: ENST00000376456.4:c.2463C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9397
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala856Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

10-24813364-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813364
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813364
    reference: chr 10
allele count: 4
allele frequency: 3.30016665841625e-5
allele num: 121206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1618C>T
  hgvsp: ENSP00000379722.1:p.His540Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1618C>T
  hgvsp: ENSP00000365634.2:p.His540Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2569C>T
  hgvsp: ENSP00000365637.3:p.His857Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1618C>T
  hgvsp: ENSP00000302343.6:p.His540Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2464C>T
  hgvsp: ENSP00000365639.4:p.His822Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1618C>T
  hgvsp: ENSP00000379723.1:p.His540Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2014C>T
  hgvsp: ENSP00000404798.1:p.His672Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2329C>T
  hgvsp: ENSP00000365645.1:p.His777Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3501C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2464C>T
  hgvsp: ENSP00000392625.1:p.His822Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2464C>T
  hgvsp: ENSP00000365635.3:p.His822Tyr
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His857Tyr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

10-24813369-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813369
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813369
    reference: chr 10
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2334C>T
  hgvsp: ENST00000376462.1:c.2334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1623C>T
  hgvsp: ENST00000307544.6:c.1623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2469C>T
  hgvsp: ENST00000376456.4:c.2469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1623C>T
  hgvsp: ENST00000396445.1:c.1623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2469C>T
  hgvsp: ENST00000376452.3:c.2469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1623C>T
  hgvsp: ENST00000396446.1:c.1623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2574C>T
  hgvsp: ENST00000376454.3:c.2574C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2019C>T
  hgvsp: ENST00000438429.1:c.2019C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2469C>T
  hgvsp: ENST00000458595.1:c.2469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1623C>T
  hgvsp: ENST00000376451.2:c.1623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3496C>T
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19383
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr858Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

10-24813371-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813371
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813371
    reference: chr 10
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1625C>T
  hgvsp: ENSP00000379722.1:p.Ser542Phe
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1625C>T
  hgvsp: ENSP00000302343.6:p.Ser542Phe
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2336C>T
  hgvsp: ENSP00000365645.1:p.Ser779Phe
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2471C>T
  hgvsp: ENSP00000392625.1:p.Ser824Phe
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3494C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2576C>T
  hgvsp: ENSP00000365637.3:p.Ser859Phe
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1625C>T
  hgvsp: ENSP00000379723.1:p.Ser542Phe
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2021C>T
  hgvsp: ENSP00000404798.1:p.Ser674Phe
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2471C>T
  hgvsp: ENSP00000365635.3:p.Ser824Phe
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2471C>T
  hgvsp: ENSP00000365639.4:p.Ser824Phe
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1625C>T
  hgvsp: ENSP00000365634.2:p.Ser542Phe
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser859Phe
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

10-24813373-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813373
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813373
    reference: chr 10
allele count: 5
allele frequency: 4.124731892426992e-5
allele num: 121220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2473G>A
  hgvsp: ENSP00000365635.3:p.Gly825Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1627G>A
  hgvsp: ENSP00000302343.6:p.Gly543Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2023G>A
  hgvsp: ENSP00000404798.1:p.Gly675Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1627G>A
  hgvsp: ENSP00000379722.1:p.Gly543Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2473G>A
  hgvsp: ENSP00000365639.4:p.Gly825Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2578G>A
  hgvsp: ENSP00000365637.3:p.Gly860Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2338G>A
  hgvsp: ENSP00000365645.1:p.Gly780Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1627G>A
  hgvsp: ENSP00000379723.1:p.Gly543Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2473G>A
  hgvsp: ENSP00000392625.1:p.Gly825Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3492G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1627G>A
  hgvsp: ENSP00000365634.2:p.Gly543Ser
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly860Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

10-24813373-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813373
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813373
    reference: chr 10
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1627G>T
  hgvsp: ENSP00000379723.1:p.Gly543Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1627G>T
  hgvsp: ENSP00000365634.2:p.Gly543Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1627G>T
  hgvsp: ENSP00000379722.1:p.Gly543Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1627G>T
  hgvsp: ENSP00000302343.6:p.Gly543Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2473G>T
  hgvsp: ENSP00000365639.4:p.Gly825Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2473G>T
  hgvsp: ENSP00000392625.1:p.Gly825Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2578G>T
  hgvsp: ENSP00000365637.3:p.Gly860Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3492G>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2023G>T
  hgvsp: ENSP00000404798.1:p.Gly675Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2338G>T
  hgvsp: ENSP00000365645.1:p.Gly780Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2473G>T
  hgvsp: ENSP00000365635.3:p.Gly825Cys
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly860Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

10-24813381-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813381
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813381
    reference: chr 10
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2481C>T
  hgvsp: ENST00000458595.1:c.2481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1635C>T
  hgvsp: ENST00000376451.2:c.1635C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2481C>T
  hgvsp: ENST00000376456.4:c.2481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1635C>T
  hgvsp: ENST00000396446.1:c.1635C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3484C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1635C>T
  hgvsp: ENST00000307544.6:c.1635C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2031C>T
  hgvsp: ENST00000438429.1:c.2031C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2586C>T
  hgvsp: ENST00000376454.3:c.2586C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1635C>T
  hgvsp: ENST00000396445.1:c.1635C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2346C>T
  hgvsp: ENST00000376462.1:c.2346C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2481C>T
  hgvsp: ENST00000376452.3:c.2481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro862Pro
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-24813394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813394
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813394
    reference: chr 10
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2359G>A
  hgvsp: ENSP00000365645.1:p.Gly787Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1648G>A
  hgvsp: ENSP00000302343.6:p.Gly550Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3471G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2044G>A
  hgvsp: ENSP00000404798.1:p.Gly682Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2494G>A
  hgvsp: ENSP00000392625.1:p.Gly832Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1648G>A
  hgvsp: ENSP00000379722.1:p.Gly550Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2599G>A
  hgvsp: ENSP00000365637.3:p.Gly867Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2494G>A
  hgvsp: ENSP00000365635.3:p.Gly832Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1648G>A
  hgvsp: ENSP00000379723.1:p.Gly550Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2494G>A
  hgvsp: ENSP00000365639.4:p.Gly832Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1648G>A
  hgvsp: ENSP00000365634.2:p.Gly550Ser
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly867Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/10-24813398-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813398
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813398
    reference: chr 10
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2498C>A
  hgvsp: ENSP00000365635.3:p.Ala833Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1652C>A
  hgvsp: ENSP00000379722.1:p.Ala551Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1652C>A
  hgvsp: ENSP00000302343.6:p.Ala551Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1652C>A
  hgvsp: ENSP00000365634.2:p.Ala551Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1652C>A
  hgvsp: ENSP00000379723.1:p.Ala551Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2498C>A
  hgvsp: ENSP00000365639.4:p.Ala833Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2498C>A
  hgvsp: ENSP00000392625.1:p.Ala833Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2603C>A
  hgvsp: ENSP00000365637.3:p.Ala868Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2048C>A
  hgvsp: ENSP00000404798.1:p.Ala683Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3467C>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2363C>A
  hgvsp: ENSP00000365645.1:p.Ala788Asp
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala868Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

10-24813398-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813398
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813398
    reference: chr 10
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2498C>G
  hgvsp: ENSP00000392625.1:p.Ala833Gly
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1652C>G
  hgvsp: ENSP00000365634.2:p.Ala551Gly
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2048C>G
  hgvsp: ENSP00000404798.1:p.Ala683Gly
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1652C>G
  hgvsp: ENSP00000379722.1:p.Ala551Gly
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1652C>G
  hgvsp: ENSP00000379723.1:p.Ala551Gly
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3467C>G
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2603C>G
  hgvsp: ENSP00000365637.3:p.Ala868Gly
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1652C>G
  hgvsp: ENSP00000302343.6:p.Ala551Gly
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2498C>G
  hgvsp: ENSP00000365639.4:p.Ala833Gly
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2498C>G
  hgvsp: ENSP00000365635.3:p.Ala833Gly
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2363C>G
  hgvsp: ENSP00000365645.1:p.Ala788Gly
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala868Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS

10-24813399-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813399
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813399
    reference: chr 10
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3466C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2499C>T
  hgvsp: ENST00000376456.4:c.2499C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2364C>T
  hgvsp: ENST00000376462.1:c.2364C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2604C>T
  hgvsp: ENST00000376454.3:c.2604C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2049C>T
  hgvsp: ENST00000438429.1:c.2049C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1653C>T
  hgvsp: ENST00000396446.1:c.1653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2499C>T
  hgvsp: ENST00000458595.1:c.2499C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1653C>T
  hgvsp: ENST00000396445.1:c.1653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1653C>T
  hgvsp: ENST00000307544.6:c.1653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1653C>T
  hgvsp: ENST00000376451.2:c.1653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2499C>T
  hgvsp: ENST00000376452.3:c.2499C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4434
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala868Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

10-24813401-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813401
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813401
    reference: chr 10
allele count: 2
allele frequency: 1.65000165000165e-5
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1655C>T
  hgvsp: ENSP00000302343.6:p.Pro552Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3464C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2501C>T
  hgvsp: ENSP00000365639.4:p.Pro834Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1655C>T
  hgvsp: ENSP00000379723.1:p.Pro552Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2606C>T
  hgvsp: ENSP00000365637.3:p.Pro869Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2366C>T
  hgvsp: ENSP00000365645.1:p.Pro789Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2501C>T
  hgvsp: ENSP00000365635.3:p.Pro834Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1655C>T
  hgvsp: ENSP00000379722.1:p.Pro552Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2501C>T
  hgvsp: ENSP00000392625.1:p.Pro834Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1655C>T
  hgvsp: ENSP00000365634.2:p.Pro552Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2051C>T
  hgvsp: ENSP00000404798.1:p.Pro684Leu
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro869Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

10-24813403-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813403
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813403
    reference: chr 10
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2053G>A
  hgvsp: ENSP00000404798.1:p.Gly685Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2503G>A
  hgvsp: ENSP00000365639.4:p.Gly835Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1657G>A
  hgvsp: ENSP00000379723.1:p.Gly553Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2503G>A
  hgvsp: ENSP00000365635.3:p.Gly835Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2368G>A
  hgvsp: ENSP00000365645.1:p.Gly790Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2503G>A
  hgvsp: ENSP00000392625.1:p.Gly835Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3462G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1657G>A
  hgvsp: ENSP00000379722.1:p.Gly553Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2608G>A
  hgvsp: ENSP00000365637.3:p.Gly870Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1657G>A
  hgvsp: ENSP00000302343.6:p.Gly553Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1657G>A
  hgvsp: ENSP00000365634.2:p.Gly553Ser
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9325
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly870Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

10-24813405-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813405
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813405
    reference: chr 10
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2505C>T
  hgvsp: ENST00000376452.3:c.2505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1659C>T
  hgvsp: ENST00000396445.1:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1659C>T
  hgvsp: ENST00000396446.1:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2370C>T
  hgvsp: ENST00000376462.1:c.2370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2610C>T
  hgvsp: ENST00000376454.3:c.2610C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2505C>T
  hgvsp: ENST00000376456.4:c.2505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1659C>T
  hgvsp: ENST00000307544.6:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2505C>T
  hgvsp: ENST00000458595.1:c.2505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1659C>T
  hgvsp: ENST00000376451.2:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2055C>T
  hgvsp: ENST00000438429.1:c.2055C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3460C>T
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly870Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum

10-24813406-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813406
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813406
    reference: chr 10
allele count: 11
allele frequency: 9.074559883845633e-5
allele num: 121218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1660G>A
  hgvsp: ENSP00000302343.6:p.Asp554Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2506G>A
  hgvsp: ENSP00000365639.4:p.Asp836Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2371G>A
  hgvsp: ENSP00000365645.1:p.Asp791Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1660G>A
  hgvsp: ENSP00000379723.1:p.Asp554Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3459G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2506G>A
  hgvsp: ENSP00000392625.1:p.Asp836Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1660G>A
  hgvsp: ENSP00000365634.2:p.Asp554Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2056G>A
  hgvsp: ENSP00000404798.1:p.Asp686Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2506G>A
  hgvsp: ENSP00000365635.3:p.Asp836Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2611G>A
  hgvsp: ENSP00000365637.3:p.Asp871Asn
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1660G>A
  hgvsp: ENSP00000379722.1:p.Asp554Asn
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp871Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

10-24813410-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813410
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813410
    reference: chr 10
allele count: 4
allele frequency: 3.299948850792813e-5
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1664C>T
  hgvsp: ENSP00000302343.6:p.Ala555Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2615C>T
  hgvsp: ENSP00000365637.3:p.Ala872Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2510C>T
  hgvsp: ENSP00000365639.4:p.Ala837Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2375C>T
  hgvsp: ENSP00000365645.1:p.Ala792Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2510C>T
  hgvsp: ENSP00000392625.1:p.Ala837Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2060C>T
  hgvsp: ENSP00000404798.1:p.Ala687Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1664C>T
  hgvsp: ENSP00000379723.1:p.Ala555Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2510C>T
  hgvsp: ENSP00000365635.3:p.Ala837Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3455C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1664C>T
  hgvsp: ENSP00000379722.1:p.Ala555Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1664C>T
  hgvsp: ENSP00000365634.2:p.Ala555Val
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9625
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala872Val
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: C
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD

10-24813411-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813411
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813411
    reference: chr 10
allele count: 27
allele frequency: 2.227318473544406e-4
allele num: 121222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2511G>A
  hgvsp: ENST00000458595.1:c.2511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1665G>A
  hgvsp: ENST00000396446.1:c.1665G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1665G>A
  hgvsp: ENST00000307544.6:c.1665G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1665G>A
  hgvsp: ENST00000396445.1:c.1665G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2376G>A
  hgvsp: ENST00000376462.1:c.2376G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2616G>A
  hgvsp: ENST00000376454.3:c.2616G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2511G>A
  hgvsp: ENST00000376456.4:c.2511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1665G>A
  hgvsp: ENST00000376451.2:c.1665G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2511G>A
  hgvsp: ENST00000376452.3:c.2511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3454G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2061G>A
  hgvsp: ENST00000438429.1:c.2061G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19482
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala872Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP

10-24813416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813416
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813416
    reference: chr 10
allele count: 2
allele frequency: 1.649947201689546e-5
allele num: 121216
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2621C>T
  hgvsp: ENSP00000365637.3:p.Ser874Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2516C>T
  hgvsp: ENSP00000392625.1:p.Ser839Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1670C>T
  hgvsp: ENSP00000365634.2:p.Ser557Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3449C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2516C>T
  hgvsp: ENSP00000365635.3:p.Ser839Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2066C>T
  hgvsp: ENSP00000404798.1:p.Ser689Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2381C>T
  hgvsp: ENSP00000365645.1:p.Ser794Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1670C>T
  hgvsp: ENSP00000302343.6:p.Ser557Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1670C>T
  hgvsp: ENSP00000379722.1:p.Ser557Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1670C>T
  hgvsp: ENSP00000379723.1:p.Ser557Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2516C>T
  hgvsp: ENSP00000365639.4:p.Ser839Leu
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser874Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-24813417-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813417
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813417
    reference: chr 10
allele count: 11
allele frequency: 9.074410163339382e-5
allele num: 121220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1671G>A
  hgvsp: ENST00000307544.6:c.1671G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2067G>A
  hgvsp: ENST00000438429.1:c.2067G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3448G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2622G>A
  hgvsp: ENST00000376454.3:c.2622G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2517G>A
  hgvsp: ENST00000458595.1:c.2517G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2382G>A
  hgvsp: ENST00000376462.1:c.2382G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1671G>A
  hgvsp: ENST00000396445.1:c.1671G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1671G>A
  hgvsp: ENST00000396446.1:c.1671G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2517G>A
  hgvsp: ENST00000376456.4:c.2517G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1671G>A
  hgvsp: ENST00000376451.2:c.1671G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2517G>A
  hgvsp: ENST00000376452.3:c.2517G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser874Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

10-24813421-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813421
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813421
    reference: chr 10
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1675G>A
  hgvsp: ENSP00000302343.6:p.Val559Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2521G>A
  hgvsp: ENSP00000365639.4:p.Val841Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1675G>A
  hgvsp: ENSP00000379722.1:p.Val559Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2521G>A
  hgvsp: ENSP00000392625.1:p.Val841Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2626G>A
  hgvsp: ENSP00000365637.3:p.Val876Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1675G>A
  hgvsp: ENSP00000365634.2:p.Val559Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1675G>A
  hgvsp: ENSP00000379723.1:p.Val559Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2386G>A
  hgvsp: ENSP00000365645.1:p.Val796Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2521G>A
  hgvsp: ENSP00000365635.3:p.Val841Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3444G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2071G>A
  hgvsp: ENSP00000404798.1:p.Val691Met
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val876Met
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/10-24813427-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813427
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813427
    reference: chr 10
allele count: 59
allele frequency: 4.866782149632929e-4
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1681C>A
  hgvsp: ENSP00000379723.1:p.Pro561Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3438C>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1681C>A
  hgvsp: ENSP00000379722.1:p.Pro561Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1681C>A
  hgvsp: ENSP00000365634.2:p.Pro561Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2077C>A
  hgvsp: ENSP00000404798.1:p.Pro693Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2527C>A
  hgvsp: ENSP00000392625.1:p.Pro843Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1681C>A
  hgvsp: ENSP00000302343.6:p.Pro561Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2527C>A
  hgvsp: ENSP00000365635.3:p.Pro843Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2392C>A
  hgvsp: ENSP00000365645.1:p.Pro798Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2632C>A
  hgvsp: ENSP00000365637.3:p.Pro878Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2527C>A
  hgvsp: ENSP00000365639.4:p.Pro843Thr
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9272
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 19476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9703
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro878Thr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

10-24813435-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813435
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813435
    reference: chr 10
allele count: 6
allele frequency: 4.949841605068638e-5
allele num: 121216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2535C>T
  hgvsp: ENST00000458595.1:c.2535C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1689C>T
  hgvsp: ENST00000396446.1:c.1689C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2535C>T
  hgvsp: ENST00000376452.3:c.2535C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2535C>T
  hgvsp: ENST00000376456.4:c.2535C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3430C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2400C>T
  hgvsp: ENST00000376462.1:c.2400C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1689C>T
  hgvsp: ENST00000396445.1:c.1689C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2640C>T
  hgvsp: ENST00000376454.3:c.2640C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1689C>T
  hgvsp: ENST00000376451.2:c.1689C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2085C>T
  hgvsp: ENST00000438429.1:c.2085C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1689C>T
  hgvsp: ENST00000307544.6:c.1689C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser880Ser
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

10-24813436-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813436
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813436
    reference: chr 10
allele count: 10
allele frequency: 8.249872126982031e-5
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1690G>A
  hgvsp: ENSP00000365634.2:p.Gly564Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2086G>A
  hgvsp: ENSP00000404798.1:p.Gly696Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1690G>A
  hgvsp: ENSP00000379722.1:p.Gly564Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2401G>A
  hgvsp: ENSP00000365645.1:p.Gly801Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1690G>A
  hgvsp: ENSP00000379723.1:p.Gly564Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2536G>A
  hgvsp: ENSP00000365639.4:p.Gly846Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2641G>A
  hgvsp: ENSP00000365637.3:p.Gly881Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2536G>A
  hgvsp: ENSP00000392625.1:p.Gly846Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1690G>A
  hgvsp: ENSP00000302343.6:p.Gly564Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2536G>A
  hgvsp: ENSP00000365635.3:p.Gly846Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3429G>A
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19468
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly881Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-24813436-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813436
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813436
    reference: chr 10
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3429G>C
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1690G>C
  hgvsp: ENSP00000379723.1:p.Gly564Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2086G>C
  hgvsp: ENSP00000404798.1:p.Gly696Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2536G>C
  hgvsp: ENSP00000392625.1:p.Gly846Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1690G>C
  hgvsp: ENSP00000379722.1:p.Gly564Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2536G>C
  hgvsp: ENSP00000365639.4:p.Gly846Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1690G>C
  hgvsp: ENSP00000302343.6:p.Gly564Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2401G>C
  hgvsp: ENSP00000365645.1:p.Gly801Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2536G>C
  hgvsp: ENSP00000365635.3:p.Gly846Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1690G>C
  hgvsp: ENSP00000365634.2:p.Gly564Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2641G>C
  hgvsp: ENSP00000365637.3:p.Gly881Arg
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19468
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly881Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

10-24813436-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813436
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813436
    reference: chr 10
allele count: 2
allele frequency: 1.649974425396406e-5
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2086G>T
  hgvsp: ENSP00000404798.1:p.Gly696Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1690G>T
  hgvsp: ENSP00000302343.6:p.Gly564Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1690G>T
  hgvsp: ENSP00000379722.1:p.Gly564Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2641G>T
  hgvsp: ENSP00000365637.3:p.Gly881Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2536G>T
  hgvsp: ENSP00000365635.3:p.Gly846Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1690G>T
  hgvsp: ENSP00000365634.2:p.Gly564Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3429G>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1690G>T
  hgvsp: ENSP00000379723.1:p.Gly564Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2536G>T
  hgvsp: ENSP00000392625.1:p.Gly846Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2401G>T
  hgvsp: ENSP00000365645.1:p.Gly801Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2536G>T
  hgvsp: ENSP00000365639.4:p.Gly846Cys
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly881Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

10-24813443-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813443
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813443
    reference: chr 10
allele count: 15
allele frequency: 1.237337908733956e-4
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2543T>C
  hgvsp: ENSP00000392625.1:p.Met848Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1697T>C
  hgvsp: ENSP00000365634.2:p.Met566Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2543T>C
  hgvsp: ENSP00000365639.4:p.Met848Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3422T>C
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2648T>C
  hgvsp: ENSP00000365637.3:p.Met883Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2408T>C
  hgvsp: ENSP00000365645.1:p.Met803Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2093T>C
  hgvsp: ENSP00000404798.1:p.Met698Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1697T>C
  hgvsp: ENSP00000302343.6:p.Met566Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1697T>C
  hgvsp: ENSP00000379723.1:p.Met566Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1697T>C
  hgvsp: ENSP00000379722.1:p.Met566Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2543T>C
  hgvsp: ENSP00000365635.3:p.Met848Thr
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9240
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Met883Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

10-24813448-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813448
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813448
    reference: chr 10
allele count: 8
allele frequency: 6.600768989587287e-5
allele num: 121198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2413C>T
  hgvsp: ENSP00000365645.1:p.Arg805Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2548C>T
  hgvsp: ENSP00000365635.3:p.Arg850Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2548C>T
  hgvsp: ENSP00000365639.4:p.Arg850Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1702C>T
  hgvsp: ENSP00000365634.2:p.Arg568Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2548C>T
  hgvsp: ENSP00000392625.1:p.Arg850Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3417C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1702C>T
  hgvsp: ENSP00000379723.1:p.Arg568Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1702C>T
  hgvsp: ENSP00000379722.1:p.Arg568Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2653C>T
  hgvsp: ENSP00000365637.3:p.Arg885Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2098C>T
  hgvsp: ENSP00000404798.1:p.Arg700Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1702C>T
  hgvsp: ENSP00000302343.6:p.Arg568Cys
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg885Cys
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-24813449-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813449
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813449
    reference: chr 10
allele count: 5
allele frequency: 4.125208323020312e-5
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2549G>A
  hgvsp: ENSP00000365635.3:p.Arg850His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1703G>A
  hgvsp: ENSP00000379723.1:p.Arg568His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2549G>A
  hgvsp: ENSP00000365639.4:p.Arg850His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1703G>A
  hgvsp: ENSP00000302343.6:p.Arg568His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1703G>A
  hgvsp: ENSP00000379722.1:p.Arg568His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2549G>A
  hgvsp: ENSP00000392625.1:p.Arg850His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2654G>A
  hgvsp: ENSP00000365637.3:p.Arg885His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2414G>A
  hgvsp: ENSP00000365645.1:p.Arg805His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2099G>A
  hgvsp: ENSP00000404798.1:p.Arg700His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3416G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1703G>A
  hgvsp: ENSP00000365634.2:p.Arg568His
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg885His
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

10-24813453-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813453
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813453
    reference: chr 10
allele count: 13
allele frequency: 1.072571862314775e-4
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1707C>T
  hgvsp: ENST00000396445.1:c.1707C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2418C>T
  hgvsp: ENST00000376462.1:c.2418C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2658C>T
  hgvsp: ENST00000376454.3:c.2658C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1707C>T
  hgvsp: ENST00000307544.6:c.1707C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2553C>T
  hgvsp: ENST00000376456.4:c.2553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1707C>T
  hgvsp: ENST00000376451.2:c.1707C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2553C>T
  hgvsp: ENST00000458595.1:c.2553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1707C>T
  hgvsp: ENST00000396446.1:c.1707C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2553C>T
  hgvsp: ENST00000376452.3:c.2553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3412C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2103C>T
  hgvsp: ENST00000438429.1:c.2103C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9224
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His886His
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

10-24813454-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813454
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813454
    reference: chr 10
allele count: 27402
allele frequency: 2.263393520889432e-1
allele num: 121066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1708G>A
  hgvsp: ENSP00000365634.2:p.Ala570Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1708G>A
  hgvsp: ENSP00000302343.6:p.Ala570Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1708G>A
  hgvsp: ENSP00000379722.1:p.Ala570Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2659G>A
  hgvsp: ENSP00000365637.3:p.Ala887Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2104G>A
  hgvsp: ENSP00000404798.1:p.Ala702Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1708G>A
  hgvsp: ENSP00000379723.1:p.Ala570Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2419G>A
  hgvsp: ENSP00000365645.1:p.Ala807Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2554G>A
  hgvsp: ENSP00000365639.4:p.Ala852Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2554G>A
  hgvsp: ENSP00000365635.3:p.Ala852Thr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3411G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2554G>A
  hgvsp: ENSP00000392625.1:p.Ala852Thr
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 4.75e1
  variant carriers: 2278
genotype depth: GenotypeDepth
  all individuals: 18122
  bin: 2.75e1
  variant carriers: 505
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 8.75e1
  variant carriers: 737
genotype depth: GenotypeDepth
  all individuals: 8240
  bin: 2.25e1
  variant carriers: 317
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 8.25e1
  variant carriers: 917
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 6.75e1
  variant carriers: 1866
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 7.75e1
  variant carriers: 1263
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 6.25e1
  variant carriers: 2054
genotype depth: GenotypeDepth
  all individuals: 7950
  bin: 3.25e1
  variant carriers: 891
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 4.25e1
  variant carriers: 1856
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 7.25e1
  variant carriers: 1500
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 5.25e1
  variant carriers: 2360
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 5.75e1
  variant carriers: 2405
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 9.75e1
  variant carriers: 3082
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.25e1
  variant carriers: 556
genotype quality: GenotypeQuality
hgvs: p.Ala887Thr
num of homozygotes: 3363
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-24813455-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813455
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813455
    reference: chr 10
allele count: 61
allele frequency: 5.033335533698594e-4
allele num: 121192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2555C>T
  hgvsp: ENSP00000365635.3:p.Ala852Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1709C>T
  hgvsp: ENSP00000379723.1:p.Ala570Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3410C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2555C>T
  hgvsp: ENSP00000392625.1:p.Ala852Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2660C>T
  hgvsp: ENSP00000365637.3:p.Ala887Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1709C>T
  hgvsp: ENSP00000365634.2:p.Ala570Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2105C>T
  hgvsp: ENSP00000404798.1:p.Ala702Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2420C>T
  hgvsp: ENSP00000365645.1:p.Ala807Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2555C>T
  hgvsp: ENSP00000365639.4:p.Ala852Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1709C>T
  hgvsp: ENSP00000379722.1:p.Ala570Val
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1709C>T
  hgvsp: ENSP00000302343.6:p.Ala570Val
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12192
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 3.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Ala887Val
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

10-24813456-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813456
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813456
    reference: chr 10
allele count: 40
allele frequency: 3.300384494793643e-4
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2421G>A
  hgvsp: ENST00000376462.1:c.2421G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3409G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1710G>A
  hgvsp: ENST00000396446.1:c.1710G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1710G>A
  hgvsp: ENST00000396445.1:c.1710G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2661G>A
  hgvsp: ENST00000376454.3:c.2661G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2556G>A
  hgvsp: ENST00000376452.3:c.2556G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1710G>A
  hgvsp: ENST00000307544.6:c.1710G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2556G>A
  hgvsp: ENST00000458595.1:c.2556G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2106G>A
  hgvsp: ENST00000438429.1:c.2106G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1710G>A
  hgvsp: ENST00000376451.2:c.1710G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2556G>A
  hgvsp: ENST00000376456.4:c.2556G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12197
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11782
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Ala887Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

10-24813462-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813462
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813462
    reference: chr 10
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2667C>T
  hgvsp: ENST00000376454.3:c.2667C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1716C>T
  hgvsp: ENST00000376451.2:c.1716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1716C>T
  hgvsp: ENST00000396445.1:c.1716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3403C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2562C>T
  hgvsp: ENST00000376452.3:c.2562C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2427C>T
  hgvsp: ENST00000376462.1:c.2427C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2562C>T
  hgvsp: ENST00000376456.4:c.2562C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2562C>T
  hgvsp: ENST00000458595.1:c.2562C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2112C>T
  hgvsp: ENST00000438429.1:c.2112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1716C>T
  hgvsp: ENST00000396446.1:c.1716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1716C>T
  hgvsp: ENST00000307544.6:c.1716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser889Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

10-24813469-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813469
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813469
    reference: chr 10
allele count: 10
allele frequency: 8.250961236984108e-5
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2119G>A
  hgvsp: ENSP00000404798.1:p.Val707Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1723G>A
  hgvsp: ENSP00000302343.6:p.Val575Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3396G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1723G>A
  hgvsp: ENSP00000379723.1:p.Val575Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2569G>A
  hgvsp: ENSP00000365639.4:p.Val857Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2434G>A
  hgvsp: ENSP00000365645.1:p.Val812Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2569G>A
  hgvsp: ENSP00000392625.1:p.Val857Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2674G>A
  hgvsp: ENSP00000365637.3:p.Val892Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1723G>A
  hgvsp: ENSP00000365634.2:p.Val575Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1723G>A
  hgvsp: ENSP00000379722.1:p.Val575Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2569G>A
  hgvsp: ENSP00000365635.3:p.Val857Met
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12114
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30028
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val892Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS

http://identifiers.org/exac.variant/10-24813475-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813475
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813475
    reference: chr 10
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1729A>C
  hgvsp: ENSP00000379722.1:p.Ile577Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1729A>C
  hgvsp: ENSP00000379723.1:p.Ile577Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2440A>C
  hgvsp: ENSP00000365645.1:p.Ile814Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2680A>C
  hgvsp: ENSP00000365637.3:p.Ile894Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1729A>C
  hgvsp: ENSP00000365634.2:p.Ile577Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2575A>C
  hgvsp: ENSP00000365635.3:p.Ile859Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2125A>C
  hgvsp: ENSP00000404798.1:p.Ile709Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3390A>C
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2575A>C
  hgvsp: ENSP00000365639.4:p.Ile859Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1729A>C
  hgvsp: ENSP00000302343.6:p.Ile577Leu
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2575A>C
  hgvsp: ENSP00000392625.1:p.Ile859Leu
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile894Leu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

10-24813476-TCCAGCCCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813476
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813467
    reference: chr 10
allele count: 4
allele frequency: 3.300547890949898e-5
allele num: 121192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsp: ENSP00000404798.1:p.Pro711_Gln713del
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsp: ENSP00000302343.6:p.Pro579_Gln581del
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsp: ENSP00000392625.1:p.Pro861_Gln863del
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsp: ENSP00000365645.1:p.Pro816_Gln818del
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsp: ENSP00000365635.3:p.Pro861_Gln863del
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsp: ENSP00000365639.4:p.Pro861_Gln863del
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsp: ENSP00000379723.1:p.Pro579_Gln581del
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsp: ENSP00000365634.2:p.Pro579_Gln581del
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsp: ENSP00000379722.1:p.Pro579_Gln581del
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsp: ENSP00000365637.3:p.Pro896_Gln898del
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 29979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12082
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro896_Gln898del
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: TCCAGCCCTC
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/10-24813479-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813479
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813479
    reference: chr 10
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1733A>C
  hgvsp: ENSP00000379723.1:p.Gln578Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2684A>C
  hgvsp: ENSP00000365637.3:p.Gln895Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2444A>C
  hgvsp: ENSP00000365645.1:p.Gln815Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2579A>C
  hgvsp: ENSP00000392625.1:p.Gln860Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1733A>C
  hgvsp: ENSP00000302343.6:p.Gln578Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2579A>C
  hgvsp: ENSP00000365639.4:p.Gln860Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2579A>C
  hgvsp: ENSP00000365635.3:p.Gln860Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1733A>C
  hgvsp: ENSP00000365634.2:p.Gln578Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1733A>C
  hgvsp: ENSP00000379722.1:p.Gln578Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3386A>C
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2129A>C
  hgvsp: ENSP00000404798.1:p.Gln710Pro
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln895Pro
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/10-24813485-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813485
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813485
    reference: chr 10
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1739C>A
  hgvsp: ENSP00000379723.1:p.Ser580Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2585C>A
  hgvsp: ENSP00000392625.1:p.Ser862Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2135C>A
  hgvsp: ENSP00000404798.1:p.Ser712Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2690C>A
  hgvsp: ENSP00000365637.3:p.Ser897Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1739C>A
  hgvsp: ENSP00000379722.1:p.Ser580Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3380C>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2585C>A
  hgvsp: ENSP00000365639.4:p.Ser862Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1739C>A
  hgvsp: ENSP00000302343.6:p.Ser580Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1739C>A
  hgvsp: ENSP00000365634.2:p.Ser580Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2585C>A
  hgvsp: ENSP00000365635.3:p.Ser862Tyr
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2450C>A
  hgvsp: ENSP00000365645.1:p.Ser817Tyr
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser897Tyr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-24813493-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813493
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813493
    reference: chr 10
allele count: 131
allele frequency: 1.081036474665786e-3
allele num: 121180
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2593T>C
  hgvsp: ENSP00000365639.4:p.Ser865Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1747T>C
  hgvsp: ENSP00000365634.2:p.Ser583Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2593T>C
  hgvsp: ENSP00000392625.1:p.Ser865Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2593T>C
  hgvsp: ENSP00000365635.3:p.Ser865Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1747T>C
  hgvsp: ENSP00000379723.1:p.Ser583Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1747T>C
  hgvsp: ENSP00000379722.1:p.Ser583Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1747T>C
  hgvsp: ENSP00000302343.6:p.Ser583Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2143T>C
  hgvsp: ENSP00000404798.1:p.Ser715Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2698T>C
  hgvsp: ENSP00000365637.3:p.Ser900Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2458T>C
  hgvsp: ENSP00000365645.1:p.Ser820Pro
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3372T>C
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11971
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 11975
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 29907
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Ser900Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-24813494-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813494
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813494
    reference: chr 10
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2594C>G
  hgvsp: ENSP00000365639.4:p.Ser865Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1748C>G
  hgvsp: ENSP00000379723.1:p.Ser583Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2594C>G
  hgvsp: ENSP00000392625.1:p.Ser865Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1748C>G
  hgvsp: ENSP00000302343.6:p.Ser583Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1748C>G
  hgvsp: ENSP00000365634.2:p.Ser583Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2459C>G
  hgvsp: ENSP00000365645.1:p.Ser820Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3371C>G
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2594C>G
  hgvsp: ENSP00000365635.3:p.Ser865Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2144C>G
  hgvsp: ENSP00000404798.1:p.Ser715Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1748C>G
  hgvsp: ENSP00000379722.1:p.Ser583Cys
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2699C>G
  hgvsp: ENSP00000365637.3:p.Ser900Cys
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29983
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser900Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

10-24813495-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813495
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813495
    reference: chr 10
allele count: 4
allele frequency: 3.301419610432486e-5
allele num: 121160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2595C>T
  hgvsp: ENST00000458595.1:c.2595C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1749C>T
  hgvsp: ENST00000376451.2:c.1749C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2595C>T
  hgvsp: ENST00000376456.4:c.2595C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1749C>T
  hgvsp: ENST00000396446.1:c.1749C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2460C>T
  hgvsp: ENST00000376462.1:c.2460C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1749C>T
  hgvsp: ENST00000307544.6:c.1749C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3370C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2700C>T
  hgvsp: ENST00000376454.3:c.2700C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2145C>T
  hgvsp: ENST00000438429.1:c.2145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1749C>T
  hgvsp: ENST00000396445.1:c.1749C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2595C>T
  hgvsp: ENST00000376452.3:c.2595C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser900Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

10-24813496-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813496
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813496
    reference: chr 10
allele count: 8
allele frequency: 6.602403274792024e-5
allele num: 121168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2596G>A
  hgvsp: ENSP00000365639.4:p.Val866Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2701G>A
  hgvsp: ENSP00000365637.3:p.Val901Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2596G>A
  hgvsp: ENSP00000392625.1:p.Val866Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2596G>A
  hgvsp: ENSP00000365635.3:p.Val866Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1750G>A
  hgvsp: ENSP00000379722.1:p.Val584Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1750G>A
  hgvsp: ENSP00000302343.6:p.Val584Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1750G>A
  hgvsp: ENSP00000379723.1:p.Val584Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2146G>A
  hgvsp: ENSP00000404798.1:p.Val716Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1750G>A
  hgvsp: ENSP00000365634.2:p.Val584Met
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3369G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2461G>A
  hgvsp: ENSP00000365645.1:p.Val821Met
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val901Met
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

10-24813498-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813498
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813498
    reference: chr 10
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2148G>A
  hgvsp: ENST00000438429.1:c.2148G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3367G>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2463G>A
  hgvsp: ENST00000376462.1:c.2463G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1752G>A
  hgvsp: ENST00000396445.1:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2598G>A
  hgvsp: ENST00000376456.4:c.2598G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2703G>A
  hgvsp: ENST00000376454.3:c.2703G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1752G>A
  hgvsp: ENST00000376451.2:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1752G>A
  hgvsp: ENST00000307544.6:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1752G>A
  hgvsp: ENST00000396446.1:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2598G>A
  hgvsp: ENST00000376452.3:c.2598G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2598G>A
  hgvsp: ENST00000458595.1:c.2598G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val901Val
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/10-24813500-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813500
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813500
    reference: chr 10
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2600C>A
  hgvsp: ENSP00000365635.3:p.Ala867Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2465C>A
  hgvsp: ENSP00000365645.1:p.Ala822Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1754C>A
  hgvsp: ENSP00000379723.1:p.Ala585Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3365C>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2600C>A
  hgvsp: ENSP00000392625.1:p.Ala867Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1754C>A
  hgvsp: ENSP00000379722.1:p.Ala585Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1754C>A
  hgvsp: ENSP00000365634.2:p.Ala585Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2600C>A
  hgvsp: ENSP00000365639.4:p.Ala867Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2705C>A
  hgvsp: ENSP00000365637.3:p.Ala902Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2150C>A
  hgvsp: ENSP00000404798.1:p.Ala717Asp
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1754C>A
  hgvsp: ENSP00000302343.6:p.Ala585Asp
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala902Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

10-24813501-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813501
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813501
    reference: chr 10
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2706C>T
  hgvsp: ENST00000376454.3:c.2706C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1755C>T
  hgvsp: ENST00000396445.1:c.1755C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2601C>T
  hgvsp: ENST00000458595.1:c.2601C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3364C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2601C>T
  hgvsp: ENST00000376452.3:c.2601C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2466C>T
  hgvsp: ENST00000376462.1:c.2466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2151C>T
  hgvsp: ENST00000438429.1:c.2151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2601C>T
  hgvsp: ENST00000376456.4:c.2601C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1755C>T
  hgvsp: ENST00000396446.1:c.1755C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1755C>T
  hgvsp: ENST00000307544.6:c.1755C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1755C>T
  hgvsp: ENST00000376451.2:c.1755C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala902Ala
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ

10-24813513-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813513
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813513
    reference: chr 10
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2163T>C
  hgvsp: ENST00000438429.1:c.2163T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2478T>C
  hgvsp: ENST00000376462.1:c.2478T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2613T>C
  hgvsp: ENST00000458595.1:c.2613T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1767T>C
  hgvsp: ENST00000396445.1:c.1767T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2718T>C
  hgvsp: ENST00000376454.3:c.2718T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2613T>C
  hgvsp: ENST00000376452.3:c.2613T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1767T>C
  hgvsp: ENST00000307544.6:c.1767T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1767T>C
  hgvsp: ENST00000376451.2:c.1767T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2613T>C
  hgvsp: ENST00000376456.4:c.2613T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1767T>C
  hgvsp: ENST00000396446.1:c.1767T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3352T>C
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro906Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

10-24813519-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813519
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813519
    reference: chr 10
allele count: 2
allele frequency: 1.650709805216243e-5
allele num: 121160
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2619G>C
  hgvsp: ENSP00000392625.1:p.Gln873His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1773G>C
  hgvsp: ENSP00000379722.1:p.Gln591His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1773G>C
  hgvsp: ENSP00000365634.2:p.Gln591His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2484G>C
  hgvsp: ENSP00000365645.1:p.Gln828His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2169G>C
  hgvsp: ENSP00000404798.1:p.Gln723His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2619G>C
  hgvsp: ENSP00000365635.3:p.Gln873His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1773G>C
  hgvsp: ENSP00000379723.1:p.Gln591His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2724G>C
  hgvsp: ENSP00000365637.3:p.Gln908His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3346G>C
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2619G>C
  hgvsp: ENSP00000365639.4:p.Gln873His
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1773G>C
  hgvsp: ENSP00000302343.6:p.Gln591His
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln908His
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

10-24813522-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813522
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813522
    reference: chr 10
allele count: 1
allele frequency: 8.253821519363466e-6
allele num: 121156
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2727C>T
  hgvsp: ENST00000376454.3:c.2727C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2622C>T
  hgvsp: ENST00000376452.3:c.2622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1776C>T
  hgvsp: ENST00000396445.1:c.1776C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2622C>T
  hgvsp: ENST00000376456.4:c.2622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2487C>T
  hgvsp: ENST00000376462.1:c.2487C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2622C>T
  hgvsp: ENST00000458595.1:c.2622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1776C>T
  hgvsp: ENST00000396446.1:c.1776C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1776C>T
  hgvsp: ENST00000376451.2:c.1776C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2172C>T
  hgvsp: ENST00000438429.1:c.2172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1776C>T
  hgvsp: ENST00000307544.6:c.1776C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3343C>T
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn909Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

10-24813526-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813526
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813526
    reference: chr 10
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3339C>T
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1780C>T
  hgvsp: ENSP00000379723.1:p.Pro594Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1780C>T
  hgvsp: ENSP00000379722.1:p.Pro594Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1780C>T
  hgvsp: ENSP00000302343.6:p.Pro594Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2176C>T
  hgvsp: ENSP00000404798.1:p.Pro726Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2626C>T
  hgvsp: ENSP00000365635.3:p.Pro876Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1780C>T
  hgvsp: ENSP00000365634.2:p.Pro594Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2626C>T
  hgvsp: ENSP00000392625.1:p.Pro876Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2731C>T
  hgvsp: ENSP00000365637.3:p.Pro911Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2626C>T
  hgvsp: ENSP00000365639.4:p.Pro876Ser
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2491C>T
  hgvsp: ENSP00000365645.1:p.Pro831Ser
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro911Ser
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

10-24813530-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813530
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813530
    reference: chr 10
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2180A>G
  hgvsp: ENSP00000404798.1:p.His727Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2495A>G
  hgvsp: ENSP00000365645.1:p.His832Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2735A>G
  hgvsp: ENSP00000365637.3:p.His912Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2630A>G
  hgvsp: ENSP00000365639.4:p.His877Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3335A>G
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1784A>G
  hgvsp: ENSP00000365634.2:p.His595Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1784A>G
  hgvsp: ENSP00000379722.1:p.His595Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1784A>G
  hgvsp: ENSP00000379723.1:p.His595Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2630A>G
  hgvsp: ENSP00000392625.1:p.His877Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2630A>G
  hgvsp: ENSP00000365635.3:p.His877Arg
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1784A>G
  hgvsp: ENSP00000302343.6:p.His595Arg
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11845
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His912Arg
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-24813531-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24813531
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 24813531
    reference: chr 10
allele count: 2
allele frequency: 1.651036851142517e-5
allele num: 121136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379723
  ensembl transcript: ENST00000396446
  gene symbol: KIAA1217
  hgvsc: ENST00000396446.1:c.1785C>A
  hgvsp: ENSP00000379723.1:p.His595Gln
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000392625
  ensembl transcript: ENST00000458595
  gene symbol: KIAA1217
  hgvsc: ENST00000458595.1:c.2631C>A
  hgvsp: ENSP00000392625.1:p.His877Gln
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365639
  ensembl transcript: ENST00000376456
  gene symbol: KIAA1217
  hgvsc: ENST00000376456.4:c.2631C>A
  hgvsp: ENSP00000365639.4:p.His877Gln
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000302343
  ensembl transcript: ENST00000307544
  gene symbol: KIAA1217
  hgvsc: ENST00000307544.6:c.1785C>A
  hgvsp: ENSP00000302343.6:p.His595Gln
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365634
  ensembl transcript: ENST00000376451
  gene symbol: KIAA1217
  hgvsc: ENST00000376451.2:c.1785C>A
  hgvsp: ENSP00000365634.2:p.His595Gln
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000379722
  ensembl transcript: ENST00000396445
  gene symbol: KIAA1217
  hgvsc: ENST00000396445.1:c.1785C>A
  hgvsp: ENSP00000379722.1:p.His595Gln
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365637
  ensembl transcript: ENST00000376454
  gene symbol: KIAA1217
  hgvsc: ENST00000376454.3:c.2736C>A
  hgvsp: ENSP00000365637.3:p.His912Gln
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365645
  ensembl transcript: ENST00000376462
  gene symbol: KIAA1217
  hgvsc: ENST00000376462.1:c.2496C>A
  hgvsp: ENSP00000365645.1:p.His832Gln
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000365635
  ensembl transcript: ENST00000376452
  gene symbol: KIAA1217
  hgvsc: ENST00000376452.3:c.2631C>A
  hgvsp: ENSP00000365635.3:p.His877Gln
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000389680
  ensembl transcript: ENST00000430453
  gene symbol: KIAA1217
  hgvsc: ENST00000430453.2:c.*-3334C>A
  variant of: http://identifiers.org/hgnc/25428
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120549
  ensembl protein: ENSP00000404798
  ensembl transcript: ENST00000438429
  gene symbol: KIAA1217
  hgvsc: ENST00000438429.1:c.2181C>A
  hgvsp: ENSP00000404798.1:p.His727Gln
  variant of: http://identifiers.org/hgnc/25428
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His912Gln
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 3665
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22416
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 8.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-1

DP
type: SiteQuality
SIO_000300: 2.405996e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.098e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 1.208e1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-1

GenotypeDepth
all individuals: 1271
bin: 7.25e1
variant carriers: 14

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 22392
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5202
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 140
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23402
bin: 9.75e1
variant carriers: 226

GenotypeQuality
all individuals: 1236
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1752
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1980
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 14
allele frequency: 1.209607741489545e-3
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 177
allele frequency: 1.702905522416779e-2
allele num: 10394
num of homozygotes: 3

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: 31
allele frequency: 4.654934230284101e-4
allele num: 66596
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.473026163463765e-4
allele num: 8638
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

DP
type: SiteQuality
SIO_000300: 2.411322e6

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

QD
type: SiteQuality
SIO_000300: 1.229e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.16e-2

FS
type: SiteQuality
SIO_000300: 5.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

VQSLOD
type: SiteQuality
SIO_000300: 4.19e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeDepth
all individuals: 671
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5220
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1240
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2351
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1985
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22465
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23268
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 1757
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.63460140537921e-4
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.801747695264407e-4
allele num: 66602
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-2

DP
type: SiteQuality
SIO_000300: 2.404693e6

VQSLOD
type: SiteQuality
SIO_000300: 3.74e0

QD
type: SiteQuality
SIO_000300: 1.033e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
all individuals: 876
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23257
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1763
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22476
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5221
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2358
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 8.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.205e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.014e0

DP
type: SiteQuality
SIO_000300: 2.404245e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

GenotypeDepth
all individuals: 3649
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

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

GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.406596e6

VQSLOD
type: SiteQuality
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QD
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SIO_000300: 1.762e1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

FS
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SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.773e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

MQ
type: SiteQuality
SIO_000300: 5.556e1

GenotypeQuality
all individuals: 127
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 84

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5212
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 66
allele frequency: 9.905150678352743e-4
allele num: 66632
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.924557351809084e-4
allele num: 10392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 13
allele frequency: 1.965527668581796e-3
allele num: 6614
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.762e1

BaseQRankSum
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SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 2.406596e6

MQRankSum
type: SiteQuality
SIO_000300: -1.773e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

MQ
type: SiteQuality
SIO_000300: 5.556e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.99e0

GenotypeDepth
all individuals: 129
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 1237
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 1967
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GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 1984
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 23212
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variant carriers: 2

GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 2355
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GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 5210
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66494
num of homozygotes: 0

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

Latino
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allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
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QD
type: SiteQuality
SIO_000300: 1.356e1

ReadPosRankSum
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SIO_000300: -3.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.289e0

DP
type: SiteQuality
SIO_000300: 2.399623e6

GenotypeDepth
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variant carriers: 10

GenotypeQuality
all individuals: 1986
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 107

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

Latino
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allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

South Asian
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allele count: 107
allele frequency: 6.480135658914729e-3
allele num: 16512
num of homozygotes: 2

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

Other
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BaseQRankSum
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SIO_000300: 3.95e0

DP
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SIO_000300: 2.408557e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
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ClippingRankSum
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QD
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FS
type: SiteQuality
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MQRankSum
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SIO_000300: 3.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.52e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

GenotypeDepth
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variant carriers: 0

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

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

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

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

South Asian
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Other
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East Asian
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allele frequency: 1.157675387821255e-4
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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FS
type: SiteQuality
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DP
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1973
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.75e1
variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66534
num of homozygotes: 0

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

South Asian
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Other
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VQSLOD
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MQRankSum
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FS
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MQ
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DP
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QD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1234
bin: 8.75e1
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GenotypeQuality
all individuals: 1972
bin: 8.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.438e1

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: -3.139e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.03e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

DP
type: SiteQuality
SIO_000300: 2.402253e6

FS
type: SiteQuality
SIO_000300: 1.197e0

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

GenotypeDepth
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variant carriers: 415

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 7

GenotypeQuality
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bin: 8.25e1
variant carriers: 22

GenotypeQuality
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variant carriers: 10

GenotypeQuality
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bin: 1.25e1
variant carriers: 2

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 145
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variant carriers: 9

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 4

GenotypeQuality
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variant carriers: 18

GenotypeQuality
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variant carriers: 9

GenotypeQuality
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variant carriers: 10

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9210

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1071
bin: 8.75e1
variant carriers: 20

European (Non-Finnish)
type: Population
allele count: 2831
allele frequency: 4.248709328851002e-2
allele num: 66632
num of homozygotes: 50

African
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allele count: 2857
allele frequency: 2.749230177059276e-1
allele num: 10392
num of homozygotes: 412

Latino
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allele count: 1184
allele frequency: 1.023867173988239e-1
allele num: 11564
num of homozygotes: 59

South Asian
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allele count: 1419
allele frequency: 8.594791035735917e-2
allele num: 16510
num of homozygotes: 74

East Asian
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allele count: 1355
allele frequency: 1.569740500463392e-1
allele num: 8632
num of homozygotes: 106

Other
type: Population
allele count: 40
allele frequency: 4.424778761061947e-2
allele num: 904
num of homozygotes: 2

European (Finnish)
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allele count: 394
allele frequency: 5.95706078016329e-2
allele num: 6614
num of homozygotes: 16

BaseQRankSum
type: SiteQuality
SIO_000300: -9.13e-1

FS
type: SiteQuality
SIO_000300: 3.284e0

QD
type: SiteQuality
SIO_000300: 1.263e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.47e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 2.477361e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 29
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 60
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GenotypeQuality
all individuals: 146
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.003121623244087e-5
allele num: 66632
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

FS
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SIO_000300: 2.441e0

MQRankSum
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SIO_000300: -2.1e-2

VQSLOD
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SIO_000300: 2.37e0

QD
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SIO_000300: 1.458e1

InbreedingCoeff
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SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 2.180652e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 2239
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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
all individuals: 2
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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: 1964
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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: 1633
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variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.78e-1

BaseQRankSum
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SIO_000300: -2.538e0

FS
type: SiteQuality
SIO_000300: 3.916e0

MQRankSum
type: SiteQuality
SIO_000300: 9.26e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 1.0e1

DP
type: SiteQuality
SIO_000300: 2.179259e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.17e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 1965
bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

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

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

East Asian
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.59e-1

FS
type: SiteQuality
SIO_000300: 2.152e0

MQ
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SIO_000300: 5.907e1

MQRankSum
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BaseQRankSum
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SIO_000300: -3.896e0

VQSLOD
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SIO_000300: -2.084e0

InbreedingCoeff
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SIO_000300: -2.0e-4

DP
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QD
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ClippingRankSum
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SIO_000300: 9.48e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 4.239341085271318e-4
allele num: 16512
num of homozygotes: 1

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

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

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

European (Non-Finnish)
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allele num: 66622
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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MQ
type: SiteQuality
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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FS
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QD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele num: 10378
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Other
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European (Finnish)
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ClippingRankSum
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BaseQRankSum
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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QD
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.005825650881355e-5
allele num: 66602
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
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SIO_000300: 4.21e-1

ClippingRankSum
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SIO_000300: -1.26e-1

FS
type: SiteQuality
SIO_000300: 6.739e0

InbreedingCoeff
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BaseQRankSum
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SIO_000300: -2.305e0

MQRankSum
type: SiteQuality
SIO_000300: -7.4e-2

MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 6.47e-1

QD
type: SiteQuality
SIO_000300: 1.122e1

DP
type: SiteQuality
SIO_000300: 2.17698e6

GenotypeDepth
all individuals: 2152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

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

Other
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.34e-1

FS
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VQSLOD
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QD
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MQ
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ClippingRankSum
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BaseQRankSum
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DP
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SIO_000300: 2.176151e6

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

QD
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SIO_000300: 1.043e1

ReadPosRankSum
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SIO_000300: 6.44e-1

DP
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MQ
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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SIO_000300: -4.53e0

FS
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

South Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 7.505704335294824e-5
allele num: 66616
num of homozygotes: 0

Other
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.283e1

VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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SIO_000300: -1.05e-1

MQRankSum
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SIO_000300: -4.6e-1

FS
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BaseQRankSum
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SIO_000300: 9.5e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

Latino
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num of homozygotes: 0

African
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allele num: 10380
num of homozygotes: 0

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

European (Finnish)
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BaseQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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MQRankSum
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FS
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InbreedingCoeff
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DP
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 0

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

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

Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66618
num of homozygotes: 0

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

European (Finnish)
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allele num: 6602
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

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

South Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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FS
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VQSLOD
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MQ
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ClippingRankSum
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SIO_000300: 9.22e-1

GenotypeDepth
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variant carriers: 0

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

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

East Asian
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European (Finnish)
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Other
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African
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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QD
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MQRankSum
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FS
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SIO_000300: 2.369e0

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

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

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66612
num of homozygotes: 0

South Asian
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Latino
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Other
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East Asian
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ReadPosRankSum
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MQRankSum
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FS
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DP
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QD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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SIO_000300: 5.964e1

GenotypeDepth
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variant carriers: 0

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

Other
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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South Asian
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VQSLOD
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BaseQRankSum
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QD
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MQ
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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FS
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8638
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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South Asian
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African
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Other
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66612
num of homozygotes: 0

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

East Asian
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allele num: 8640
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Latino
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South Asian
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European (Non-Finnish)
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European (Finnish)
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African
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ReadPosRankSum
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MQ
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InbreedingCoeff
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SIO_000300: 2.4e-3

BaseQRankSum
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SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: 7.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.108e0

DP
type: SiteQuality
SIO_000300: 2.175398e6

FS
type: SiteQuality
SIO_000300: 3.071e0

QD
type: SiteQuality
SIO_000300: 1.334e1

VQSLOD
type: SiteQuality
SIO_000300: 9.58e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 27

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.004563468235859e-5
allele num: 66616
num of homozygotes: 0

Latino
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allele count: 22
allele frequency: 1.90179806362379e-3
allele num: 11568
num of homozygotes: 0

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

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

East Asian
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BaseQRankSum
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SIO_000300: -4.5e-1

MQ
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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QD
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FS
type: SiteQuality
SIO_000300: 1.753e0

DP
type: SiteQuality
SIO_000300: 2.175568e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 1.516990291262136e-4
allele num: 6592
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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VQSLOD
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DP
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FS
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MQ
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SIO_000300: 5.937e1

QD
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SIO_000300: 8.65e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

GenotypeDepth
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11

European (Non-Finnish)
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allele count: 3
allele frequency: 4.503422601176894e-5
allele num: 66616
num of homozygotes: 0

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

African
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allele count: 6
allele frequency: 5.775895263765884e-4
allele num: 10388
num of homozygotes: 0

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

South Asian
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allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e-1

QD
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DP
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InbreedingCoeff
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SIO_000300: 1.0e-4

MQRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: 9.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.813e1

VQSLOD
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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DP
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SIO_000300: 2.174557e6

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 59

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

East Asian
type: Population
allele count: 23
allele frequency: 2.662037037037037e-3
allele num: 8640
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 32
allele frequency: 4.802929787170174e-4
allele num: 66626
num of homozygotes: 0

South Asian
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allele frequency: 1.817300702689605e-4
allele num: 16508
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BaseQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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ClippingRankSum
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FS
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Other
type: Population
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European (Finnish)
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African
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allele count: 2
allele frequency: 1.926040061633282e-4
allele num: 10384
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.503017021404341e-5
allele num: 66622
num of homozygotes: 0

East Asian
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Latino
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InbreedingCoeff
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MQ
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DP
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FS
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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allele num: 16508
num of homozygotes: 0

African
type: Population
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allele frequency: 9.632055480639569e-5
allele num: 10382
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Latino
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allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

European (Finnish)
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East Asian
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allele frequency: 2.314279102059708e-4
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European (Non-Finnish)
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allele frequency: 7.505028369007235e-5
allele num: 66622
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Other
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MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
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ClippingRankSum
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DP
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QD
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MQRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

GenotypeDepth
all individuals: 755
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17183
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1187
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1925
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 27168
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6138
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 202
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.729e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 2.176138e6

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

QD
type: SiteQuality
SIO_000300: 1.402e1

GenotypeDepth
all individuals: 19468
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 120
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1621
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27168
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17183
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 202
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1925
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2200
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002011347602894e-5
allele num: 66622
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.951e1

MQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

DP
type: SiteQuality
SIO_000300: 2.176138e6

QD
type: SiteQuality
SIO_000300: 1.402e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 1.729e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

GenotypeDepth
all individuals: 3790
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1188
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27123
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2507
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6125
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2201
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1617
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17178
bin: 9.75e1
variant carriers: 15

Latino
type: Population
allele count: 3
allele frequency: 2.593809441466367e-4
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.80099054479964e-4
allele num: 66630
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

FS
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 2.175296e6

GenotypeDepth
all individuals: 2147
bin: 5.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 1616
bin: 9.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 26958
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1917
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 209
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17173
bin: 9.75e1
variant carriers: 7

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

GenotypeQuality
all individuals: 119
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6093
bin: 6.75e1
variant carriers: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.006574799603711e-5
allele num: 66618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.912e0

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

QD
type: SiteQuality
SIO_000300: 1.449e1

DP
type: SiteQuality
SIO_000300: 2.174479e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-2

GenotypeDepth
all individuals: 4405
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 213
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2495
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26905
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 17176
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1183
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6081
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817300702689605e-4
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001921229586936e-5
allele num: 66624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.99e-1

FS
type: SiteQuality
SIO_000300: 3.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.337e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.091e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

DP
type: SiteQuality
SIO_000300: 2.174439e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

GenotypeDepth
all individuals: 4403
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27003
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6079
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1925
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2497
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1613
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 17186
bin: 9.75e1
variant carriers: 12

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

GenotypeQuality
all individuals: 2193
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 6
allele frequency: 5.781460782424359e-4
allele num: 10378
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.505478999669759e-5
allele num: 66618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.44e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.242e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.728e0

MQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.174292e6

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

GenotypeDepth
all individuals: 2968
bin: 3.75e1
variant carriers: 1276

GenotypeQuality
all individuals: 935
bin: 8.25e1
variant carriers: 49

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 7

GenotypeQuality
all individuals: 4974
bin: 6.75e1
variant carriers: 23

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 8

GenotypeQuality
all individuals: 97
bin: 5.75e1
variant carriers: 22

GenotypeQuality
all individuals: 88
bin: 3.75e1
variant carriers: 7

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 25184
bin: 9.75e1
variant carriers: 23724

GenotypeQuality
all individuals: 1509
bin: 7.75e1
variant carriers: 41

GenotypeQuality
all individuals: 114
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 13

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 170
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 24785
bin: 6.25e1
variant carriers: 17

GenotypeQuality
all individuals: 1450
bin: 7.25e1
variant carriers: 33

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 16

GenotypeQuality
all individuals: 406
bin: 8.75e1
variant carriers: 37

GenotypeQuality
all individuals: 521
bin: 9.25e1
variant carriers: 50

South Asian
type: Population
allele count: 2302
allele frequency: 1.394644371743608e-1
allele num: 16506
num of homozygotes: 161

European (Finnish)
type: Population
allele count: 1381
allele frequency: 2.101339013998783e-1
allele num: 6572
num of homozygotes: 143

East Asian
type: Population
allele count: 928
allele frequency: 1.076815966581573e-1
allele num: 8618
num of homozygotes: 48

Latino
type: Population
allele count: 1785
allele frequency: 1.545989953230556e-1
allele num: 11546
num of homozygotes: 135

Other
type: Population
allele count: 211
allele frequency: 2.339246119733925e-1
allele num: 902
num of homozygotes: 29

African
type: Population
allele count: 2440
allele frequency: 2.352033930981299e-1
allele num: 10374
num of homozygotes: 299

European (Non-Finnish)
type: Population
allele count: 18355
allele frequency: 2.758159523952636e-1
allele num: 66548
num of homozygotes: 2548

QD
type: SiteQuality
SIO_000300: 1.682e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.78e-1

DP
type: SiteQuality
SIO_000300: 2.634421e6

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

FS
type: SiteQuality
SIO_000300: 5.21e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.63e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.21e-1

GenotypeDepth
all individuals: 694
bin: 4.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2465
bin: 7.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 61

GenotypeQuality
all individuals: 139
bin: 5.25e1
variant carriers: 0

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

Other
type: Population
allele count: 2
allele frequency: 2.217294900221729e-3
allele num: 902
num of homozygotes: 0

East Asian
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allele count: 58
allele frequency: 6.709856547894493e-3
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -7.0e-4

MQRankSum
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SIO_000300: 1.4e-2

VQSLOD
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SIO_000300: 2.91e0

ClippingRankSum
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SIO_000300: -3.79e-1

BaseQRankSum
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SIO_000300: -7.94e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

FS
type: SiteQuality
SIO_000300: 1.743e0

ReadPosRankSum
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SIO_000300: 5.88e-1

DP
type: SiteQuality
SIO_000300: 1.734578e6

QD
type: SiteQuality
SIO_000300: 1.258e1

GenotypeDepth
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variant carriers: 2

GenotypeQuality
all individuals: 107
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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
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.503152206544582e-5
allele num: 66620
num of homozygotes: 0

Latino
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allele count: 34
allele frequency: 2.941176470588235e-3
allele num: 11560
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.637625289128758e-5
allele num: 10376
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

VQSLOD
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SIO_000300: 3.45e0

MQ
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SIO_000300: 5.974e1

QD
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InbreedingCoeff
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SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-2

DP
type: SiteQuality
SIO_000300: 1.733337e6

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

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

Other
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allele num: 904
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

South Asian
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allele count: 0
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BaseQRankSum
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SIO_000300: -2.222e0

MQ
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SIO_000300: 6.0e1

VQSLOD
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MQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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SIO_000300: -2.7e-2

FS
type: SiteQuality
SIO_000300: 3.963e0

QD
type: SiteQuality
SIO_000300: 1.067e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
all individuals: 793
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
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allele count: 10
allele frequency: 9.63948332369385e-4
allele num: 10374
num of homozygotes: 0

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

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

Other
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ClippingRankSum
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SIO_000300: -4.76e-1

VQSLOD
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SIO_000300: 5.21e0

MQRankSum
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DP
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InbreedingCoeff
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SIO_000300: 3.4e-3

ReadPosRankSum
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QD
type: SiteQuality
SIO_000300: 1.339e1

MQ
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SIO_000300: 5.954e1

BaseQRankSum
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SIO_000300: -3.302e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

East Asian
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Other
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MQRankSum
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SIO_000300: 4.62e-1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.004563468235859e-5
allele num: 66616
num of homozygotes: 0

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

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

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

African
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East Asian
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.077e1

DP
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SIO_000300: 1.725176e6

MQRankSum
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SIO_000300: 1.2e-1

BaseQRankSum
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SIO_000300: -5.03e-1

MQ
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SIO_000300: 5.938e1

InbreedingCoeff
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SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.505e0

VQSLOD
type: SiteQuality
SIO_000300: 6.8e-1

ClippingRankSum
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SIO_000300: 8.500000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

GenotypeDepth
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variant carriers: 11

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 130

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

European (Non-Finnish)
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allele count: 111
allele frequency: 1.666516530042339e-3
allele num: 66606
num of homozygotes: 0

Latino
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allele frequency: 2.595155709342561e-4
allele num: 11560
num of homozygotes: 0

African
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num of homozygotes: 0

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

European (Finnish)
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allele count: 15
allele frequency: 2.276867030965392e-3
allele num: 6588
num of homozygotes: 0

Other
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allele num: 904
num of homozygotes: 0

MQ
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SIO_000300: 5.962e1

DP
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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SIO_000300: -1.06e-1

ReadPosRankSum
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MQRankSum
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QD
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InbreedingCoeff
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SIO_000300: -1.3e-3

BaseQRankSum
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SIO_000300: 1.48e0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.288e0

MQRankSum
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SIO_000300: -9.6e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
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SIO_000300: 8.38e-1

ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.720615e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00318337437684e-5
allele num: 66596
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

VQSLOD
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MQRankSum
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ClippingRankSum
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MQ
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SIO_000300: 5.957e1

QD
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FS
type: SiteQuality
SIO_000300: 5.25e-1

BaseQRankSum
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SIO_000300: 1.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
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SIO_000300: 1.720506e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

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

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

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

European (Finnish)
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allele count: 1
allele frequency: 1.517911353976928e-4
allele num: 6588
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.050987928652934e-4
allele num: 66604
num of homozygotes: 0

South Asian
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VQSLOD
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SIO_000300: 1.05e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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East Asian
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South Asian
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BaseQRankSum
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MQ
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ClippingRankSum
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DP
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MQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
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East Asian
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European (Non-Finnish)
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QD
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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Other
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European (Non-Finnish)
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East Asian
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European (Finnish)
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South Asian
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FS
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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DP
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66596
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Latino
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Other
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African
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East Asian
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South Asian
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European (Finnish)
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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MQ
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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Other
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Latino
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African
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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FS
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DP
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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DP
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VQSLOD
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ReadPosRankSum
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FS
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Non-Finnish)
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South Asian
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African
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European (Finnish)
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Latino
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ClippingRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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QD
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MQ
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MQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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