2-8926065-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926065
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926065
    reference: chr 2
allele count: 1
allele frequency: 8.28363154406892e-6
allele num: 120720
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1909A>G
  hgvsp: ENSP00000414923.1:p.Ile637Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.2035A>G
  hgvsp: ENSP00000411849.1:p.Ile679Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.2035A>G
  hgvsp: ENSP00000256707.3:p.Ile679Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1276A>G
  hgvsp: ENSP00000420364.1:p.Ile426Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.2035A>G
  hgvsp: ENSP00000418974.1:p.Ile679Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.2038A>G
  hgvsp: ENSP00000419964.1:p.Ile680Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.2038A>G
  hgvsp: ENSP00000319947.5:p.Ile680Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2095A>G
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3493
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2429
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25182
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile679Val
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

2-8926080-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926080
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926080
    reference: chr 2
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.2020A>G
  hgvsp: ENSP00000256707.3:p.Ile674Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.2023A>G
  hgvsp: ENSP00000419964.1:p.Ile675Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.2023A>G
  hgvsp: ENSP00000319947.5:p.Ile675Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2080A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1261A>G
  hgvsp: ENSP00000420364.1:p.Ile421Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.2020A>G
  hgvsp: ENSP00000411849.1:p.Ile674Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.2020A>G
  hgvsp: ENSP00000418974.1:p.Ile674Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1894A>G
  hgvsp: ENSP00000414923.1:p.Ile632Val
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3492
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile674Val
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum

2-8926088-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926088
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926088
    reference: chr 2
allele count: 2
allele frequency: 1.657797450307521e-5
allele num: 120642
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1886T>C
  hgvsp: ENSP00000414923.1:p.Ile629Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.2012T>C
  hgvsp: ENSP00000411849.1:p.Ile671Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.2015T>C
  hgvsp: ENSP00000419964.1:p.Ile672Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.2015T>C
  hgvsp: ENSP00000319947.5:p.Ile672Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1253T>C
  hgvsp: ENSP00000420364.1:p.Ile418Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.2012T>C
  hgvsp: ENSP00000256707.3:p.Ile671Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2072T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.2012T>C
  hgvsp: ENSP00000418974.1:p.Ile671Thr
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2428
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25151
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11797
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile671Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-8926089-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926089
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926089
    reference: chr 2
allele count: 1
allele frequency: 8.28953694646617e-6
allele num: 120634
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.2011A>G
  hgvsp: ENSP00000418974.1:p.Ile671Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.2011A>G
  hgvsp: ENSP00000411849.1:p.Ile671Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2071A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1885A>G
  hgvsp: ENSP00000414923.1:p.Ile629Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.2011A>G
  hgvsp: ENSP00000256707.3:p.Ile671Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1252A>G
  hgvsp: ENSP00000420364.1:p.Ile418Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.2014A>G
  hgvsp: ENSP00000319947.5:p.Ile672Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.2014A>G
  hgvsp: ENSP00000419964.1:p.Ile672Val
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2428
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11795
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3315
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile671Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

2-8926090-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926090
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926090
    reference: chr 2
allele count: 8
allele frequency: 6.632949175026946e-5
allele num: 120610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.2013T>C
  hgvsp: ENST00000319688.5:c.2013T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.2010T>C
  hgvsp: ENST00000473731.1:c.2010T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2070T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.2013T>C
  hgvsp: ENST00000489024.1:c.2013T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1884T>C
  hgvsp: ENST00000418530.1:c.1884T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.2010T>C
  hgvsp: ENST00000427284.1:c.2010T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.2010T>C
  hgvsp: ENST00000256707.3:c.2010T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1251T>C
  hgvsp: ENST00000496383.1:c.1251T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3488
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11797
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 3311
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile670Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/2-8926098-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926098
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926098
    reference: chr 2
allele count: 1
allele frequency: 8.29462508294625e-6
allele num: 120560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.2002G>T
  hgvsp: ENSP00000418974.1:p.Gly668Cys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.2005G>T
  hgvsp: ENSP00000319947.5:p.Gly669Cys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.2002G>T
  hgvsp: ENSP00000256707.3:p.Gly668Cys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.2005G>T
  hgvsp: ENSP00000419964.1:p.Gly669Cys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2062G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1876G>T
  hgvsp: ENSP00000414923.1:p.Gly626Cys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.2002G>T
  hgvsp: ENSP00000411849.1:p.Gly668Cys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1243G>T
  hgvsp: ENSP00000420364.1:p.Gly415Cys
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7689
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4471
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly668Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

2-8926100-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926100
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926100
    reference: chr 2
allele count: 6
allele frequency: 4.977435625165914e-5
allele num: 120544
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.2003T>C
  hgvsp: ENSP00000419964.1:p.Ile668Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.2000T>C
  hgvsp: ENSP00000411849.1:p.Ile667Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1241T>C
  hgvsp: ENSP00000420364.1:p.Ile414Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1874T>C
  hgvsp: ENSP00000414923.1:p.Ile625Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2060T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.2000T>C
  hgvsp: ENSP00000256707.3:p.Ile667Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.2003T>C
  hgvsp: ENSP00000319947.5:p.Ile668Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.2000T>C
  hgvsp: ENSP00000418974.1:p.Ile667Thr
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3483
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7692
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile667Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

2-8926104-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926104
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926104
    reference: chr 2
allele count: 3
allele frequency: 2.490411914130597e-5
allele num: 120462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1999A>C
  hgvsp: ENSP00000419964.1:p.Ile667Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1999A>C
  hgvsp: ENSP00000319947.5:p.Ile667Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1237A>C
  hgvsp: ENSP00000420364.1:p.Ile413Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1870A>C
  hgvsp: ENSP00000414923.1:p.Ile624Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1996A>C
  hgvsp: ENSP00000411849.1:p.Ile666Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2056A>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1996A>C
  hgvsp: ENSP00000256707.3:p.Ile666Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1996A>C
  hgvsp: ENSP00000418974.1:p.Ile666Leu
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3296
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile666Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

2-8926120-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926120
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926120
    reference: chr 2
allele count: 1
allele frequency: 8.348081610845828e-6
allele num: 119788
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1980T>C
  hgvsp: ENST00000256707.3:c.1980T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1983T>C
  hgvsp: ENST00000319688.5:c.1983T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1854T>C
  hgvsp: ENST00000418530.1:c.1854T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1983T>C
  hgvsp: ENST00000489024.1:c.1983T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2040T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1980T>C
  hgvsp: ENST00000427284.1:c.1980T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1980T>C
  hgvsp: ENST00000473731.1:c.1980T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1221T>C
  hgvsp: ENST00000496383.1:c.1221T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3265
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe660Phe
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

2-8926123-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926123
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926123
    reference: chr 2
allele count: 5
allele frequency: 4.180392288012307e-5
allele num: 119606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1977T>A
  hgvsp: ENST00000473731.1:c.1977T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1980T>A
  hgvsp: ENST00000489024.1:c.1980T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1980T>A
  hgvsp: ENST00000319688.5:c.1980T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1851T>A
  hgvsp: ENST00000418530.1:c.1851T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1977T>A
  hgvsp: ENST00000256707.3:c.1977T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1218T>A
  hgvsp: ENST00000496383.1:c.1218T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1977T>A
  hgvsp: ENST00000427284.1:c.1977T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2037T>A
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23978
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2427
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser659Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

2-8926125-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926125
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926125
    reference: chr 2
allele count: 8
allele frequency: 6.704434983741745e-5
allele num: 119324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1849T>A
  hgvsp: ENSP00000414923.1:p.Ser617Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1216T>A
  hgvsp: ENSP00000420364.1:p.Ser406Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1975T>A
  hgvsp: ENSP00000418974.1:p.Ser659Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1978T>A
  hgvsp: ENSP00000319947.5:p.Ser660Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1975T>A
  hgvsp: ENSP00000256707.3:p.Ser659Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1978T>A
  hgvsp: ENSP00000419964.1:p.Ser660Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2035T>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1975T>A
  hgvsp: ENSP00000411849.1:p.Ser659Thr
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19362
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11841
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6244
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3468
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2426
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23565
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4435
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser659Thr
num of homozygotes: 1
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

2-8926126-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926126
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926126
    reference: chr 2
allele count: 2
allele frequency: 1.676024469957262e-5
allele num: 119330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1848A>G
  hgvsp: ENST00000418530.1:c.1848A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1215A>G
  hgvsp: ENST00000496383.1:c.1215A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2034A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1974A>G
  hgvsp: ENST00000427284.1:c.1974A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1977A>G
  hgvsp: ENST00000489024.1:c.1977A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1977A>G
  hgvsp: ENST00000319688.5:c.1977A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1974A>G
  hgvsp: ENST00000256707.3:c.1974A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1974A>G
  hgvsp: ENST00000473731.1:c.1974A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23624
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3264
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro658Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

2-8926131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926131
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926131
    reference: chr 2
allele count: 2
allele frequency: 1.683643404326963e-5
allele num: 118790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1972C>T
  hgvsp: ENSP00000319947.5:p.Leu658Phe
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1969C>T
  hgvsp: ENSP00000418974.1:p.Leu657Phe
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1972C>T
  hgvsp: ENSP00000419964.1:p.Leu658Phe
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1969C>T
  hgvsp: ENSP00000256707.3:p.Leu657Phe
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2029C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1969C>T
  hgvsp: ENSP00000411849.1:p.Leu657Phe
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1843C>T
  hgvsp: ENSP00000414923.1:p.Leu615Phe
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1210C>T
  hgvsp: ENSP00000420364.1:p.Leu404Phe
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11768
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2424
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu657Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-8926169-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926169
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926169
    reference: chr 2
allele count: 2
allele frequency: 1.756913454443234e-5
allele num: 113836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1940-9G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1814-9G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1943-9G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1940-9G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1943-9G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1940-9G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2000-9G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1181-9G>T
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4436
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

2-8926176-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926176
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926176
    reference: chr 2
allele count: 7
allele frequency: 6.18702492487184e-5
allele num: 113140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1940-16A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1181-16A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2000-16A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1943-16A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1940-16A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1940-16A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1814-16A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1943-16A>G
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15721
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4640
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6283
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11738
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 4181
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

2-8926196-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926196
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926196
    reference: chr 2
allele count: 2
allele frequency: 1.801087857065668e-5
allele num: 111044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1940-36A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1943-36A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1181-36A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2000-36A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1814-36A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1940-36A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1940-36A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1943-36A>G
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12095
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7549
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11730
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11673
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

2-8926202-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926202
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926202
    reference: chr 2
allele count: 2
allele frequency: 1.81047905275736e-5
allele num: 110468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1814-42T>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1940-42T>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1943-42T>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*2000-42T>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1940-42T>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1943-42T>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1940-42T>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1181-42T>A
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5972
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1213
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2841
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/2-8926295-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926295
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926295
    reference: chr 2
allele count: 1
allele frequency: 8.332222370350619e-6
allele num: 120016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1939+41G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1813+41G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1942+41G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1999+41G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1939+41G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1180+41G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1942+41G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1939+41G>T
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2853
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5742
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

2-8926304-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926304
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926304
    reference: chr 2
allele count: 5
allele frequency: 4.162088369460261e-5
allele num: 120132
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1813+32A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1942+32A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1942+32A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1939+32A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1939+32A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1939+32A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1999+32A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1180+32A>G
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6822
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6611
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

2-8926313-A-AGAAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926313
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926317
    reference: chr 2
allele count: 1
allele frequency: 8.316838270762986e-6
allele num: 120238
alternate allele: AGAAG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1939+19_1939+22dupCTTC
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1942+19_1942+22dupCTTC
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1180+19_1180+22dupCTTC
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1939+19_1939+22dupCTTC
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1939+19_1939+22dupCTTC
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1942+19_1942+22dupCTTC
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1999+19_*1999+22dupCTTC
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1813+19_1813+22dupCTTC
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2852
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39060
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

2-8926318-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926318
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926318
    reference: chr 2
allele count: 1
allele frequency: 8.313795912937929e-6
allele num: 120282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1939+18C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1999+18C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1180+18C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1939+18C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1942+18C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1939+18C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1942+18C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1813+18C>T
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6825
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39059
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2852
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2573
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

2-8926333-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926333
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926333
    reference: chr 2
allele count: 3
allele frequency: 2.489957172736629e-5
allele num: 120484
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1813+3A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1939+3A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1939+3A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1939+3A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1942+3A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1180+3A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1942+3A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1999+3A>G
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5550
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2217
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1939+3A>G
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

2-8926341-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926341
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926341
    reference: chr 2
allele count: 62
allele frequency: 5.14514281920632e-4
allele num: 120502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1937C>T
  hgvsp: ENSP00000419964.1:p.Thr646Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1994C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1175C>T
  hgvsp: ENSP00000420364.1:p.Thr392Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1808C>T
  hgvsp: ENSP00000414923.1:p.Thr603Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1934C>T
  hgvsp: ENSP00000411849.1:p.Thr645Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1934C>T
  hgvsp: ENSP00000418974.1:p.Thr645Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1937C>T
  hgvsp: ENSP00000319947.5:p.Thr646Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1934C>T
  hgvsp: ENSP00000256707.3:p.Thr645Ile
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 9.75e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39073
  bin: 9.75e1
  variant carriers: 61
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr645Ile
num of homozygotes: 1
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

2-8926349-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926349
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926349
    reference: chr 2
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1926T>C
  hgvsp: ENST00000473731.1:c.1926T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1929T>C
  hgvsp: ENST00000319688.5:c.1929T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1986T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1929T>C
  hgvsp: ENST00000489024.1:c.1929T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1800T>C
  hgvsp: ENST00000418530.1:c.1800T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1926T>C
  hgvsp: ENST00000427284.1:c.1926T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1926T>C
  hgvsp: ENST00000256707.3:c.1926T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1167T>C
  hgvsp: ENST00000496383.1:c.1167T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39056
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2850
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr642Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

2-8926363-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926363
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926363
    reference: chr 2
allele count: 1
allele frequency: 8.296964970213896e-6
allele num: 120526
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1912C>T
  hgvsp: ENSP00000256707.3:p.Arg638Ter
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1915C>T
  hgvsp: ENSP00000419964.1:p.Arg639Ter
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1912C>T
  hgvsp: ENSP00000418974.1:p.Arg638Ter
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1153C>T
  hgvsp: ENSP00000420364.1:p.Arg385Ter
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1786C>T
  hgvsp: ENSP00000414923.1:p.Arg596Ter
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1915C>T
  hgvsp: ENSP00000319947.5:p.Arg639Ter
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1912C>T
  hgvsp: ENSP00000411849.1:p.Arg638Ter
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1972C>T
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6830
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2638
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg638Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

2-8926375-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926375
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926375
    reference: chr 2
allele count: 2
allele frequency: 1.659282857948795e-5
allele num: 120534
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1774A>G
  hgvsp: ENSP00000414923.1:p.Thr592Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1900A>G
  hgvsp: ENSP00000418974.1:p.Thr634Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1141A>G
  hgvsp: ENSP00000420364.1:p.Thr381Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1900A>G
  hgvsp: ENSP00000256707.3:p.Thr634Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1903A>G
  hgvsp: ENSP00000319947.5:p.Thr635Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1960A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1903A>G
  hgvsp: ENSP00000419964.1:p.Thr635Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1900A>G
  hgvsp: ENSP00000411849.1:p.Thr634Ala
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2643
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2201
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr634Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

2-8926376-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926376
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926376
    reference: chr 2
allele count: 1
allele frequency: 8.296689620841284e-6
allele num: 120530
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1899A>T
  hgvsp: ENST00000427284.1:c.1899A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1899A>T
  hgvsp: ENST00000256707.3:c.1899A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1959A>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1773A>T
  hgvsp: ENST00000418530.1:c.1773A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1902A>T
  hgvsp: ENST00000489024.1:c.1902A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1899A>T
  hgvsp: ENST00000473731.1:c.1899A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1902A>T
  hgvsp: ENST00000319688.5:c.1902A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1140A>T
  hgvsp: ENST00000496383.1:c.1140A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala633Ala
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

2-8926385-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926385
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926385
    reference: chr 2
allele count: 1
allele frequency: 8.29737802854298e-6
allele num: 120520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1893C>G
  hgvsp: ENST00000319688.5:c.1893C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1131C>G
  hgvsp: ENST00000496383.1:c.1131C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1890C>G
  hgvsp: ENST00000256707.3:c.1890C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1890C>G
  hgvsp: ENST00000473731.1:c.1890C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1890C>G
  hgvsp: ENST00000427284.1:c.1890C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1893C>G
  hgvsp: ENST00000489024.1:c.1893C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1950C>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1764C>G
  hgvsp: ENST00000418530.1:c.1764C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly630Gly
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

2-8926407-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926407
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926407
    reference: chr 2
allele count: 1
allele frequency: 8.301510874979247e-6
allele num: 120460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1928A>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1871A>T
  hgvsp: ENSP00000319947.5:p.Asp624Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1868A>T
  hgvsp: ENSP00000418974.1:p.Asp623Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1742A>T
  hgvsp: ENSP00000414923.1:p.Asp581Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1109A>T
  hgvsp: ENSP00000420364.1:p.Asp370Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1868A>T
  hgvsp: ENSP00000256707.3:p.Asp623Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1868A>T
  hgvsp: ENSP00000411849.1:p.Asp623Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1871A>T
  hgvsp: ENSP00000419964.1:p.Asp624Val
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8132
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp623Val
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

2-8926417-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926417
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926417
    reference: chr 2
allele count: 11
allele frequency: 9.134695233349942e-5
allele num: 120420
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1732A>G
  hgvsp: ENSP00000414923.1:p.Thr578Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1861A>G
  hgvsp: ENSP00000419964.1:p.Thr621Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1099A>G
  hgvsp: ENSP00000420364.1:p.Thr367Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1858A>G
  hgvsp: ENSP00000256707.3:p.Thr620Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1861A>G
  hgvsp: ENSP00000319947.5:p.Thr621Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1918A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1858A>G
  hgvsp: ENSP00000411849.1:p.Thr620Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1858A>G
  hgvsp: ENSP00000418974.1:p.Thr620Ala
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2849
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2624
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr620Ala
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

2-8926425-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926425
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926425
    reference: chr 2
allele count: 1
allele frequency: 8.30675172780436e-6
allele num: 120384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1724T>C
  hgvsp: ENSP00000414923.1:p.Met575Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1853T>C
  hgvsp: ENSP00000419964.1:p.Met618Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1853T>C
  hgvsp: ENSP00000319947.5:p.Met618Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1850T>C
  hgvsp: ENSP00000411849.1:p.Met617Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1910T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1850T>C
  hgvsp: ENSP00000418974.1:p.Met617Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1091T>C
  hgvsp: ENSP00000420364.1:p.Met364Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1850T>C
  hgvsp: ENSP00000256707.3:p.Met617Thr
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2620
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2850
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Met617Thr
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

2-8926433-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926433
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926433
    reference: chr 2
allele count: 1
allele frequency: 8.311722853913159e-6
allele num: 120312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1845G>A
  hgvsp: ENST00000489024.1:c.1845G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1842G>A
  hgvsp: ENST00000427284.1:c.1842G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1083G>A
  hgvsp: ENST00000496383.1:c.1083G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1842G>A
  hgvsp: ENST00000473731.1:c.1842G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1902G>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1845G>A
  hgvsp: ENST00000319688.5:c.1845G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1716G>A
  hgvsp: ENST00000418530.1:c.1716G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1842G>A
  hgvsp: ENST00000256707.3:c.1842G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2199
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1246
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2850
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu614Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

2-8926435-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926435
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926435
    reference: chr 2
allele count: 1
allele frequency: 8.31282835672009e-6
allele num: 120296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1843C>G
  hgvsp: ENSP00000419964.1:p.Leu615Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1843C>G
  hgvsp: ENSP00000319947.5:p.Leu615Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1840C>G
  hgvsp: ENSP00000256707.3:p.Leu614Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1714C>G
  hgvsp: ENSP00000414923.1:p.Leu572Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1840C>G
  hgvsp: ENSP00000411849.1:p.Leu614Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1900C>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1081C>G
  hgvsp: ENSP00000420364.1:p.Leu361Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1840C>G
  hgvsp: ENSP00000418974.1:p.Leu614Val
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39054
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2199
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu614Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP

2-8926462-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926462
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926462
    reference: chr 2
allele count: 1
allele frequency: 8.332222370350619e-6
allele num: 120016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1816C>T
  hgvsp: ENST00000489024.1:c.1816C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1813C>T
  hgvsp: ENST00000256707.3:c.1813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1813C>T
  hgvsp: ENST00000473731.1:c.1813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1873C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1687C>T
  hgvsp: ENST00000418530.1:c.1687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1054C>T
  hgvsp: ENST00000496383.1:c.1054C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1816C>T
  hgvsp: ENST00000319688.5:c.1816C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1813C>T
  hgvsp: ENST00000427284.1:c.1813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7888
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu605Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

2-8926467-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926467
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926467
    reference: chr 2
allele count: 3
allele frequency: 2.500833611203735e-5
allele num: 119960
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1808A>G
  hgvsp: ENSP00000418974.1:p.Asn603Ser
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1049A>G
  hgvsp: ENSP00000420364.1:p.Asn350Ser
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1868A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1811A>G
  hgvsp: ENSP00000319947.5:p.Asn604Ser
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1682A>G
  hgvsp: ENSP00000414923.1:p.Asn561Ser
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1808A>G
  hgvsp: ENSP00000411849.1:p.Asn603Ser
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1808A>G
  hgvsp: ENSP00000256707.3:p.Asn603Ser
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1811A>G
  hgvsp: ENSP00000419964.1:p.Asn604Ser
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1244
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn603Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

2-8926469-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926469
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926469
    reference: chr 2
allele count: 5
allele frequency: 4.169098640873843e-5
allele num: 119930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1680C>T
  hgvsp: ENST00000418530.1:c.1680C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1866C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1809C>T
  hgvsp: ENST00000319688.5:c.1809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1047C>T
  hgvsp: ENST00000496383.1:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1806C>T
  hgvsp: ENST00000427284.1:c.1806C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1809C>T
  hgvsp: ENST00000489024.1:c.1809C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1806C>T
  hgvsp: ENST00000473731.1:c.1806C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1806C>T
  hgvsp: ENST00000256707.3:c.1806C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2601
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr602Tyr
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

2-8926479-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926479
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926479
    reference: chr 2
allele count: 1
allele frequency: 8.345852111500584e-6
allele num: 119820
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1670T>A
  hgvsp: ENSP00000414923.1:p.Phe557Tyr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1796T>A
  hgvsp: ENSP00000256707.3:p.Phe599Tyr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1799T>A
  hgvsp: ENSP00000319947.5:p.Phe600Tyr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1796T>A
  hgvsp: ENSP00000411849.1:p.Phe599Tyr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1856T>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1799T>A
  hgvsp: ENSP00000419964.1:p.Phe600Tyr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1796T>A
  hgvsp: ENSP00000418974.1:p.Phe599Tyr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1037T>A
  hgvsp: ENSP00000420364.1:p.Phe346Tyr
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39050
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Phe599Tyr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

2-8926481-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926481
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926481
    reference: chr 2
allele count: 1
allele frequency: 8.348360382020972e-6
allele num: 119784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1668G>A
  hgvsp: ENST00000418530.1:c.1668G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1797G>A
  hgvsp: ENST00000319688.5:c.1797G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1794G>A
  hgvsp: ENST00000427284.1:c.1794G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1797G>A
  hgvsp: ENST00000489024.1:c.1797G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1035G>A
  hgvsp: ENST00000496383.1:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1794G>A
  hgvsp: ENST00000256707.3:c.1794G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1794G>A
  hgvsp: ENST00000473731.1:c.1794G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1854G>A
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu598Leu
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

2-8926493-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926493
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926493
    reference: chr 2
allele count: 3
allele frequency: 2.507354907729339e-5
allele num: 119648
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1791-6T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1788-6T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1662-6T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1788-6T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1788-6T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1029-6T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1848-6T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1791-6T>C
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6485
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2851
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1788-6T>C
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

2-8926508-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926508
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926508
    reference: chr 2
allele count: 4
allele frequency: 3.349747094094396e-5
allele num: 119412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1788-21T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1791-21T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1029-21T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1848-21T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1788-21T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1788-21T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1791-21T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1662-21T>C
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2401
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/2-8926509-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926509
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926509
    reference: chr 2
allele count: 7
allele frequency: 5.862646566164154e-5
allele num: 119400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1788-22T>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1791-22T>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1029-22T>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1848-22T>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1662-22T>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1791-22T>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1788-22T>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1788-22T>G
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6982
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 1
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ

2-8926509-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926509
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926509
    reference: chr 2
allele count: 1
allele frequency: 8.375209380234507e-6
allele num: 119400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1791-22T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1788-22T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1029-22T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1662-22T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1791-22T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1788-22T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1848-22T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1788-22T>C
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6435
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

2-8926512-ATTACT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926512
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926507
    reference: chr 2
allele count: 1
allele frequency: 8.380403265005112e-6
allele num: 119326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1848-30_*1848-26delAGTAA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1029-30_1029-26delAGTAA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1791-30_1791-26delAGTAA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1791-30_1791-26delAGTAA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1788-30_1788-26delAGTAA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1788-30_1788-26delAGTAA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1662-30_1662-26delAGTAA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1788-30_1788-26delAGTAA
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6830
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2474
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: ATTACT
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

2-8926522-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926522
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926522
    reference: chr 2
allele count: 1
allele frequency: 8.38841727342885e-6
allele num: 119212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1788-35A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1662-35A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1788-35A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1791-35A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1791-35A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1848-35A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1029-35A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1788-35A>G
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1202
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2395
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2853
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

2-8926530-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8926530
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8926530
    reference: chr 2
allele count: 1
allele frequency: 8.394050297149381e-6
allele num: 119132
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1662-43C>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1848-43C>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1788-43C>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1791-43C>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1791-43C>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1029-43C>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1788-43C>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1788-43C>G
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5291
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4746
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

2-8928738-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928738
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928738
    reference: chr 2
allele count: 4
allele frequency: 3.391612542183181e-5
allele num: 117938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+39A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+39A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+39A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+39A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+39A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+39A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+39A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+39A>G
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14134
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7615
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3124
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

2-8928739-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928739
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928739
    reference: chr 2
allele count: 1
allele frequency: 8.487667419239845e-6
allele num: 117818
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+38G>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+38G>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+38G>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+38G>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+38G>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+38G>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+38G>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+38G>A
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12291
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

2-8928740-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928740
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928740
    reference: chr 2
allele count: 2
allele frequency: 1.695691248537466e-5
allele num: 117946
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+37A>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+37A>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+37A>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+37A>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+37A>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+37A>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+37A>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+37A>C
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2711
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

2-8928743-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928743
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928743
    reference: chr 2
allele count: 2
allele frequency: 1.6933653943848e-5
allele num: 118108
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+34A>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+34A>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+34A>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+34A>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+34A>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+34A>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+34A>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+34A>T
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16051
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1236
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

2-8928743-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928743
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928743
    reference: chr 2
allele count: 8
allele frequency: 6.773461577539202e-5
allele num: 118108
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+34A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+34A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+34A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+34A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+34A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+34A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+34A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+34A>G
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20199
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7674
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

2-8928749-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928749
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928749
    reference: chr 2
allele count: 1
allele frequency: 8.439958137807636e-6
allele num: 118484
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+28T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+28T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+28T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+28T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+28T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+28T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+28T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+28T>C
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7730
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

2-8928749-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928749
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928748
    reference: chr 2
allele count: 1
allele frequency: 8.439958137807636e-6
allele num: 118484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+27delA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+27delA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+27delA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+27delA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+27delA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+27delA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+27delA
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+27delA
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12281
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4885
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: AT
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-8928753-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928753
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928753
    reference: chr 2
allele count: 45
allele frequency: 3.792923248090896e-4
allele num: 118642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+24G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+24G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+24G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+24G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+24G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+24G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+24G>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+24G>T
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7278
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16270
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7746
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21203
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3159
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

2-8928758-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928758
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928758
    reference: chr 2
allele count: 7
allele frequency: 5.881166823497782e-5
allele num: 119024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+19C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+19C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+19C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+19C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+19C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+19C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+19C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+19C>T
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16416
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4898
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2717
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

2-8928758-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928758
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928758
    reference: chr 2
allele count: 1
allele frequency: 8.401666890711118e-6
allele num: 119024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+19C>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+19C>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+19C>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+19C>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+19C>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+19C>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+19C>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+19C>A
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16416
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2717
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3168
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7798
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21640
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

2-8928765-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928765
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928765
    reference: chr 2
allele count: 1
allele frequency: 8.371563473194253e-6
allele num: 119452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+12C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+12C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+12C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+12C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+12C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+12C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+12C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+12C>T
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2718
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

2-8928770-A-AACTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928770
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928774
    reference: chr 2
allele count: 1
allele frequency: 8.352544184958738e-6
allele num: 119724
alternate allele: AACTC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1661+3_1661+6dupGAGT
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1790+3_1790+6dupGAGT
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1787+3_1787+6dupGAGT
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1790+3_1790+6dupGAGT
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1847+3_*1847+6dupGAGT
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1787+3_1787+6dupGAGT
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1787+3_1787+6dupGAGT
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1028+3_1028+6dupGAGT
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3191
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1787+3_1787+6dupGAGT
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/2-8928782-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928782
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928782
    reference: chr 2
allele count: 1
allele frequency: 8.319190709127816e-6
allele num: 120204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1023T>G
  hgvsp: ENST00000496383.1:c.1023T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1656T>G
  hgvsp: ENST00000418530.1:c.1656T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1785T>G
  hgvsp: ENST00000489024.1:c.1785T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1842T>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1782T>G
  hgvsp: ENST00000427284.1:c.1782T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1782T>G
  hgvsp: ENST00000473731.1:c.1782T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1785T>G
  hgvsp: ENST00000319688.5:c.1785T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1782T>G
  hgvsp: ENST00000256707.3:c.1782T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22677
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3999
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro594Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

2-8928783-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928783
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928783
    reference: chr 2
allele count: 1
allele frequency: 8.319190709127816e-6
allele num: 120204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1784C>T
  hgvsp: ENSP00000319947.5:p.Pro595Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1841C>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1781C>T
  hgvsp: ENSP00000411849.1:p.Pro594Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1655C>T
  hgvsp: ENSP00000414923.1:p.Pro552Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1784C>T
  hgvsp: ENSP00000419964.1:p.Pro595Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.1022C>T
  hgvsp: ENSP00000420364.1:p.Pro341Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1781C>T
  hgvsp: ENSP00000418974.1:p.Pro594Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1781C>T
  hgvsp: ENSP00000256707.3:p.Pro594Leu
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14337
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7939
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3198
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro594Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/2-8928810-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928810
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928810
    reference: chr 2
allele count: 2
allele frequency: 1.657989853102099e-5
allele num: 120628
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.995T>G
  hgvsp: ENSP00000420364.1:p.Leu332Trp
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1754T>G
  hgvsp: ENSP00000418974.1:p.Leu585Trp
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1757T>G
  hgvsp: ENSP00000419964.1:p.Leu586Trp
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1628T>G
  hgvsp: ENSP00000414923.1:p.Leu543Trp
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1754T>G
  hgvsp: ENSP00000256707.3:p.Leu585Trp
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1757T>G
  hgvsp: ENSP00000319947.5:p.Leu586Trp
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1754T>G
  hgvsp: ENSP00000411849.1:p.Leu585Trp
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1814T>G
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4915
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3990
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu585Trp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-8928814-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928814
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928814
    reference: chr 2
allele count: 1
allele frequency: 8.288987251537607e-6
allele num: 120642
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1750G>A
  hgvsp: ENSP00000256707.3:p.Glu584Lys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1753G>A
  hgvsp: ENSP00000319947.5:p.Glu585Lys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1624G>A
  hgvsp: ENSP00000414923.1:p.Glu542Lys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1750G>A
  hgvsp: ENSP00000411849.1:p.Glu584Lys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1810G>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1750G>A
  hgvsp: ENSP00000418974.1:p.Glu584Lys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1753G>A
  hgvsp: ENSP00000419964.1:p.Glu585Lys
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.991G>A
  hgvsp: ENSP00000420364.1:p.Glu331Lys
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3194
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu584Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

2-8928827-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928827
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928827
    reference: chr 2
allele count: 6
allele frequency: 4.971661529283086e-5
allele num: 120684
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1737T>C
  hgvsp: ENST00000256707.3:c.1737T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1740T>C
  hgvsp: ENST00000489024.1:c.1740T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1611T>C
  hgvsp: ENST00000418530.1:c.1611T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.978T>C
  hgvsp: ENST00000496383.1:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1737T>C
  hgvsp: ENST00000427284.1:c.1737T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1797T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1740T>C
  hgvsp: ENST00000319688.5:c.1740T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1737T>C
  hgvsp: ENST00000473731.1:c.1737T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3193
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe579Phe
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

2-8928829-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928829
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928829
    reference: chr 2
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1609T>A
  hgvsp: ENSP00000414923.1:p.Phe537Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1795T>A
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1735T>A
  hgvsp: ENSP00000411849.1:p.Phe579Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1738T>A
  hgvsp: ENSP00000419964.1:p.Phe580Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.976T>A
  hgvsp: ENSP00000420364.1:p.Phe326Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1738T>A
  hgvsp: ENSP00000319947.5:p.Phe580Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1735T>A
  hgvsp: ENSP00000256707.3:p.Phe579Ile
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1735T>A
  hgvsp: ENSP00000418974.1:p.Phe579Ile
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Phe579Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

2-8928832-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928832
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928832
    reference: chr 2
allele count: 3
allele frequency: 2.485789569626966e-5
allele num: 120686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1606A>T
  hgvsp: ENSP00000414923.1:p.Met536Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1732A>T
  hgvsp: ENSP00000411849.1:p.Met578Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1732A>T
  hgvsp: ENSP00000418974.1:p.Met578Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1735A>T
  hgvsp: ENSP00000419964.1:p.Met579Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.973A>T
  hgvsp: ENSP00000420364.1:p.Met325Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1735A>T
  hgvsp: ENSP00000319947.5:p.Met579Leu
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1792A>T
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1732A>T
  hgvsp: ENSP00000256707.3:p.Met578Leu
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met578Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

2-8928833-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928833
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928833
    reference: chr 2
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1605G>A
  hgvsp: ENST00000418530.1:c.1605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1731G>A
  hgvsp: ENST00000473731.1:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1734G>A
  hgvsp: ENST00000489024.1:c.1734G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1734G>A
  hgvsp: ENST00000319688.5:c.1734G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.972G>A
  hgvsp: ENST00000496383.1:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1731G>A
  hgvsp: ENST00000256707.3:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1731G>A
  hgvsp: ENST00000427284.1:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1791G>A
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3193
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu577Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-8928835-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928835
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928835
    reference: chr 2
allele count: 4
allele frequency: 3.314111486710413e-5
allele num: 120696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1732T>C
  hgvsp: ENST00000489024.1:c.1732T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.970T>C
  hgvsp: ENST00000496383.1:c.970T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1603T>C
  hgvsp: ENST00000418530.1:c.1603T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1729T>C
  hgvsp: ENST00000473731.1:c.1729T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1732T>C
  hgvsp: ENST00000319688.5:c.1732T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1729T>C
  hgvsp: ENST00000427284.1:c.1729T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1789T>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1729T>C
  hgvsp: ENST00000256707.3:c.1729T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7987
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu577Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

2-8928857-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928857
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928857
    reference: chr 2
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1767A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1707A>G
  hgvsp: ENST00000256707.3:c.1707A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1707A>G
  hgvsp: ENST00000473731.1:c.1707A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1710A>G
  hgvsp: ENST00000319688.5:c.1710A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1707A>G
  hgvsp: ENST00000427284.1:c.1707A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1710A>G
  hgvsp: ENST00000489024.1:c.1710A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1581A>G
  hgvsp: ENST00000418530.1:c.1581A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.948A>G
  hgvsp: ENST00000496383.1:c.948A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7984
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly569Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

2-8928858-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928858
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928858
    reference: chr 2
allele count: 1
allele frequency: 8.284180528862085e-6
allele num: 120712
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1706G>C
  hgvsp: ENSP00000411849.1:p.Gly569Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1706G>C
  hgvsp: ENSP00000256707.3:p.Gly569Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.947G>C
  hgvsp: ENSP00000420364.1:p.Gly316Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1709G>C
  hgvsp: ENSP00000419964.1:p.Gly570Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1706G>C
  hgvsp: ENSP00000418974.1:p.Gly569Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1766G>C
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1709G>C
  hgvsp: ENSP00000319947.5:p.Gly570Ala
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1580G>C
  hgvsp: ENSP00000414923.1:p.Gly527Ala
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7983
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly569Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/2-8928860-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928860
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928860
    reference: chr 2
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1704T>G
  hgvsp: ENSP00000256707.3:p.Ile568Met
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.945T>G
  hgvsp: ENSP00000420364.1:p.Ile315Met
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1707T>G
  hgvsp: ENSP00000319947.5:p.Ile569Met
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1704T>G
  hgvsp: ENSP00000418974.1:p.Ile568Met
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1578T>G
  hgvsp: ENSP00000414923.1:p.Ile526Met
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1707T>G
  hgvsp: ENSP00000419964.1:p.Ile569Met
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1764T>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1704T>G
  hgvsp: ENSP00000411849.1:p.Ile568Met
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14381
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1816
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3196
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3987
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile568Met
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

2-8928861-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928861
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928861
    reference: chr 2
allele count: 2
allele frequency: 1.656918463042434e-5
allele num: 120706
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1706T>C
  hgvsp: ENSP00000419964.1:p.Ile569Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1703T>C
  hgvsp: ENSP00000418974.1:p.Ile568Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.944T>C
  hgvsp: ENSP00000420364.1:p.Ile315Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1577T>C
  hgvsp: ENSP00000414923.1:p.Ile526Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1703T>C
  hgvsp: ENSP00000411849.1:p.Ile568Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1706T>C
  hgvsp: ENSP00000319947.5:p.Ile569Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1703T>C
  hgvsp: ENSP00000256707.3:p.Ile568Thr
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1763T>C
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3987
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1816
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3196
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile568Thr
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

2-8928862-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8928862
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 8928862
    reference: chr 2
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000319947
  ensembl transcript: ENST00000319688
  gene symbol: KIDINS220
  hgvsc: ENST00000319688.5:c.1705A>G
  hgvsp: ENSP00000319947.5:p.Ile569Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000411849
  ensembl transcript: ENST00000427284
  gene symbol: KIDINS220
  hgvsc: ENST00000427284.1:c.1702A>G
  hgvsp: ENSP00000411849.1:p.Ile568Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000419964
  ensembl transcript: ENST00000489024
  gene symbol: KIDINS220
  hgvsc: ENST00000489024.1:c.1705A>G
  hgvsp: ENSP00000419964.1:p.Ile569Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000418974
  ensembl transcript: ENST00000473731
  gene symbol: KIDINS220
  hgvsc: ENST00000473731.1:c.1702A>G
  hgvsp: ENSP00000418974.1:p.Ile568Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000417390
  ensembl transcript: ENST00000488729
  gene symbol: KIDINS220
  hgvsc: ENST00000488729.1:c.*1762A>G
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000414923
  ensembl transcript: ENST00000418530
  gene symbol: KIDINS220
  hgvsc: ENST00000418530.1:c.1576A>G
  hgvsp: ENSP00000414923.1:p.Ile526Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000256707
  ensembl transcript: ENST00000256707
  gene symbol: KIDINS220
  hgvsc: ENST00000256707.3:c.1702A>G
  hgvsp: ENSP00000256707.3:p.Ile568Val
  variant of: http://identifiers.org/hgnc/29508
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134313
  ensembl protein: ENSP00000420364
  ensembl transcript: ENST00000496383
  gene symbol: KIDINS220
  hgvsc: ENST00000496383.1:c.943A>G
  hgvsp: ENSP00000420364.1:p.Ile315Val
  variant of: http://identifiers.org/hgnc/29508
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17594
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile568Val
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4483
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11801
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3321
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1738
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.949e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

VQSLOD
type: SiteQuality
SIO_000300: -1.089e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.442e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.33e0

DP
type: SiteQuality
SIO_000300: 2.118107e6

QD
type: SiteQuality
SIO_000300: 1.548e1

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7721
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3318
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11799
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 1739
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25159
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4483
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 9.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.07e0

DP
type: SiteQuality
SIO_000300: 2.117614e6

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.29e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 5.574e0

QD
type: SiteQuality
SIO_000300: 1.407e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3489
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7710
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3313
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4479
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1738
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212709192335678e-4
allele num: 16492
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.572e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 8.372e0

DP
type: SiteQuality
SIO_000300: 2.117002e6

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: -5.373e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

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

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

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

GenotypeQuality
all individuals: 3489
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1737
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25158
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4478
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7710
bin: 6.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.020616452337212e-4
allele num: 9798
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.737e0

MQRankSum
type: SiteQuality
SIO_000300: -4.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.98e-1

DP
type: SiteQuality
SIO_000300: 2.11697e6

QD
type: SiteQuality
SIO_000300: 1.307e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

GenotypeQuality
all individuals: 25083
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7700
bin: 6.75e1
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: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4475
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.213739531496541e-4
allele num: 16478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.500975126766479e-5
allele num: 66658
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 5.268e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.48e0

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.116768e6

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

QD
type: SiteQuality
SIO_000300: 1.457e1

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

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3483
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2427
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11788
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25085
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.0790273556231e-5
allele num: 16450
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.917e1

DP
type: SiteQuality
SIO_000300: 2.115787e6

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

FS
type: SiteQuality
SIO_000300: 1.263e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.332e0

VQSLOD
type: SiteQuality
SIO_000300: -4.561e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.396e0

QD
type: SiteQuality
SIO_000300: 9.31e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 5
allele frequency: 5.105166428425567e-4
allele num: 9794
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
SIO_000300: 1.752e0

QD
type: SiteQuality
SIO_000300: 1.438e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

DP
type: SiteQuality
SIO_000300: 2.115437e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.021450459652707e-4
allele num: 9790
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002101471029721e-5
allele num: 66620
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

FS
type: SiteQuality
SIO_000300: 1.334e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.114647e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.87e-1

GenotypeQuality
all individuals: 967
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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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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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
all individuals: 11779
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variant carriers: 1

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.273525721455458e-5
allele num: 15940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66432
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.957e1

FS
type: SiteQuality
SIO_000300: 1.2512e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e0

DP
type: SiteQuality
SIO_000300: 2.103063e6

VQSLOD
type: SiteQuality
SIO_000300: -3.959e0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.78e-1

QD
type: SiteQuality
SIO_000300: 1.339e1

GenotypeQuality
all individuals: 3467
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3260
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GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.02571860816944e-4
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.518888955835392e-5
allele num: 66388
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 7.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-2

FS
type: SiteQuality
SIO_000300: 5.34e-1

DP
type: SiteQuality
SIO_000300: 2.099852e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.277e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 1.405e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
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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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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11781
bin: 9.75e1
variant carriers: 7

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 5.119017148707448e-4
allele num: 15628
num of homozygotes: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66296
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -4.72e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 1.578e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.25e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

QD
type: SiteQuality
SIO_000300: 1.61e1

MQRankSum
type: SiteQuality
SIO_000300: 5.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.6e-1

DP
type: SiteQuality
SIO_000300: 2.094778e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 198
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variant carriers: 0

GenotypeQuality
all individuals: 4437
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 2.04582651391162e-4
allele num: 9776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15632
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.281e1

DP
type: SiteQuality
SIO_000300: 2.094705e6

FS
type: SiteQuality
SIO_000300: 3.394e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.176e0

MQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.73e-1

GenotypeQuality
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bin: 8.75e1
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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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 2.049600327936052e-4
allele num: 9758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

FS
type: SiteQuality
SIO_000300: 6.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.492e0

QD
type: SiteQuality
SIO_000300: 1.145e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

DP
type: SiteQuality
SIO_000300: 2.084888e6

MQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.2e-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
all individuals: 17902
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547316952404531e-5
allele num: 64628
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.036269430051813e-4
allele num: 9650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12312
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

QD
type: SiteQuality
SIO_000300: 1.112e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.29e-1

FS
type: SiteQuality
SIO_000300: 1.896e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.509e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.57e-1

DP
type: SiteQuality
SIO_000300: 1.996985e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 518
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GenotypeQuality
all individuals: 189
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 7
allele frequency: 7.264425072644251e-4
allele num: 9636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11940
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.04e1

DP
type: SiteQuality
SIO_000300: 1.971733e6

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.207e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

FS
type: SiteQuality
SIO_000300: 5.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1693
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.143171460003143e-5
allele num: 63630
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 1.908664e6

VQSLOD
type: SiteQuality
SIO_000300: -2.883e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

QD
type: SiteQuality
SIO_000300: 1.503e1

FS
type: SiteQuality
SIO_000300: 9.577e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10792
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.158859020121932e-5
allele num: 63314
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.197e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.396e1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

DP
type: SiteQuality
SIO_000300: 1.898799e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

FS
type: SiteQuality
SIO_000300: 1.218e0

MQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 44
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.112845e6

QD
type: SiteQuality
SIO_000300: 1.654e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.377e0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.171e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.61e0

FS
type: SiteQuality
SIO_000300: 3.448e0

VQSLOD
type: SiteQuality
SIO_000300: -2.837e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 457
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.730702665282105e-4
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.518752824220515e-5
allele num: 66390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16338
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

DP
type: SiteQuality
SIO_000300: 3.120349e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.87e-1

QD
type: SiteQuality
SIO_000300: 1.527e1

FS
type: SiteQuality
SIO_000300: 2.192e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.28e0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2406
bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.027749229188078e-4
allele num: 9730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66422
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: -1.284e0

QD
type: SiteQuality
SIO_000300: 1.356e1

DP
type: SiteQuality
SIO_000300: 3.127515e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.888e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.399999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.905e1

FS
type: SiteQuality
SIO_000300: 6.833e0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9724
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66454
num of homozygotes: 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: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.31e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.029e0

FS
type: SiteQuality
SIO_000300: 6.985e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 3.13053e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.11e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.596952908587258e-4
allele num: 11552
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

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

QD
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.654e0

BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e0

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 45
allele frequency: 5.220417633410673e-3
allele num: 8620
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

Latino
type: Population
allele count: 17
allele frequency: 1.471861471861472e-3
allele num: 11550
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
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FS
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BaseQRankSum
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DP
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2404
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
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

MQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

MQ
type: SiteQuality
SIO_000300: 5.988e1

QD
type: SiteQuality
SIO_000300: 1.209e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.638e0

FS
type: SiteQuality
SIO_000300: 5.625e0

DP
type: SiteQuality
SIO_000300: 3.136495e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 39055
bin: 9.75e1
variant carriers: 1

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.515e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.659e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.53e-1

QD
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VQSLOD
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SIO_000300: -2.317e0

MQRankSum
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SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 3.137077e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.74e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
type: SiteQuality
SIO_000300: 1.24e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.48e-1

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

DP
type: SiteQuality
SIO_000300: 3.137316e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.305e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.748e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.377e1

DP
type: SiteQuality
SIO_000300: 3.137252e6

FS
type: SiteQuality
SIO_000300: 1.604e0

VQSLOD
type: SiteQuality
SIO_000300: 9.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 3.137099e6

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.294e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.863e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.325e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66584
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
allele num: 900
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FS
type: SiteQuality
SIO_000300: 1.237e0

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
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BaseQRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.868e0

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 1.029654036243822e-4
allele num: 9712
num of homozygotes: 0

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

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

Latino
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allele frequency: 1.733102253032929e-4
allele num: 11540
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 8
allele frequency: 1.201886962531174e-4
allele num: 66562
num of homozygotes: 0

QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 5.28e-1

DP
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502900598154438e-5
allele num: 66538
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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FS
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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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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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66490
num of homozygotes: 0

Latino
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allele frequency: 8.667013347200555e-5
allele num: 11538
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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FS
type: SiteQuality
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QD
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MQ
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.026e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.16e-1

QD
type: SiteQuality
SIO_000300: 1.478e1

MQRankSum
type: SiteQuality
SIO_000300: -1.131e0

VQSLOD
type: SiteQuality
SIO_000300: -6.054e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

FS
type: SiteQuality
SIO_000300: 9.010999999999999e0

DP
type: SiteQuality
SIO_000300: 3.134763e6

GenotypeQuality
all individuals: 500
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507886245061673e-5
allele num: 66318
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9614
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.75e-1

FS
type: SiteQuality
SIO_000300: 4.075e0

DP
type: SiteQuality
SIO_000300: 3.131687e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.07e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.29e-1

QD
type: SiteQuality
SIO_000300: 1.33e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

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

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.822600243013366e-4
allele num: 16460
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66270
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.09e0

FS
type: SiteQuality
SIO_000300: 1.6025e1

MQ
type: SiteQuality
SIO_000300: 5.921e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.011e0

DP
type: SiteQuality
SIO_000300: 3.131119e6

MQRankSum
type: SiteQuality
SIO_000300: -4.65e-1

QD
type: SiteQuality
SIO_000300: 1.472e1

VQSLOD
type: SiteQuality
SIO_000300: -2.186e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.038100413609878e-5
allele num: 66246
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.932e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 3.130966e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

MQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

QD
type: SiteQuality
SIO_000300: 1.296e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.418e0

GenotypeQuality
all individuals: 1244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 595
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GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510802235987309e-5
allele num: 66190
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.129102e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.674e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 9.73e-1

FS
type: SiteQuality
SIO_000300: 2.252e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: -2.698e0

QD
type: SiteQuality
SIO_000300: 2.327e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.165501165501166e-4
allele num: 8580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

MQRankSum
type: SiteQuality
SIO_000300: -9.23e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 1.4369e1

QD
type: SiteQuality
SIO_000300: 9.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.823e0

DP
type: SiteQuality
SIO_000300: 3.12864e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9556
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66090
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.825928180158247e-4
allele num: 16430
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.71e-1

FS
type: SiteQuality
SIO_000300: 3.539e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.961e0

MQRankSum
type: SiteQuality
SIO_000300: -5.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.289e1

DP
type: SiteQuality
SIO_000300: 3.126372e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65958
num of homozygotes: 0

African
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allele count: 4
allele frequency: 4.201680672268908e-4
allele num: 9520
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.4e-2

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.423e1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65950
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9522
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.27141811081279e-4
allele num: 16388
num of homozygotes: 1

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

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

MQRankSum
type: SiteQuality
SIO_000300: 9.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.655e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

DP
type: SiteQuality
SIO_000300: 3.119892e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeQuality
all individuals: 6982
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39050
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516300227445034e-5
allele num: 65950
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9522
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.85e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

QD
type: SiteQuality
SIO_000300: 1.655e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 3.119892e6

GenotypeQuality
all individuals: 2398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

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: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 7.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517174414370676e-5
allele num: 65912
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: -5.258e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.195e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 5.357e1

DP
type: SiteQuality
SIO_000300: 3.115763e6

QD
type: SiteQuality
SIO_000300: 8.029999999999999e0

GenotypeQuality
all individuals: 2388
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2177
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variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 39046
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1469
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5678
bin: 6.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518741267237713e-5
allele num: 65844
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: -2.062e0

VQSLOD
type: SiteQuality
SIO_000300: -1.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.106683e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.551e1

GenotypeQuality
all individuals: 2288
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 139
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2168
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variant carriers: 0

GenotypeQuality
all individuals: 2853
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 317
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variant carriers: 0

GenotypeQuality
all individuals: 39045
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variant carriers: 1

GenotypeQuality
all individuals: 2383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519895431194334e-5
allele num: 65794
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9492
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.098787e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
SIO_000300: -3.611e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.939e1

MQRankSum
type: SiteQuality
SIO_000300: 8.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.24e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
all individuals: 12296
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 995
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 360
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variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 593
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variant carriers: 0

GenotypeQuality
all individuals: 1812
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variant carriers: 0

GenotypeQuality
all individuals: 3988
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
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variant carriers: 0

GenotypeQuality
all individuals: 2715
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variant carriers: 0

GenotypeQuality
all individuals: 4866
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variant carriers: 0

GenotypeQuality
all individuals: 19229
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.075334143377886e-5
allele num: 65840
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e0

DP
type: SiteQuality
SIO_000300: 2.092095e6

FS
type: SiteQuality
SIO_000300: 9.330000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

MQRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.92e-1

QD
type: SiteQuality
SIO_000300: 1.502e1

GenotypeQuality
all individuals: 19392
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 302
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2711
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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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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1286
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4861
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variant carriers: 0

GenotypeQuality
all individuals: 587
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variant carriers: 0

GenotypeQuality
all individuals: 7602
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65824
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.75949709341625e-5
allele num: 14794
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.382e0

MQRankSum
type: SiteQuality
SIO_000300: -1.455e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.693e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.126e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.43e0

QD
type: SiteQuality
SIO_000300: 4.98e0

DP
type: SiteQuality
SIO_000300: 2.094213e6

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 70
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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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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1813
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3131
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19570
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73973556019485e-4
allele num: 11496
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14882
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 1.291e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

FS
type: SiteQuality
SIO_000300: 1.329e0

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.061e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.59e-1

DP
type: SiteQuality
SIO_000300: 2.095824e6

GenotypeQuality
all individuals: 7674
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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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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2710
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3988
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.1441647597254e-3
allele num: 874
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14976
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65906
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.69414014953921e-5
allele num: 11502
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 2.102384e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

QD
type: SiteQuality
SIO_000300: 1.383e1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.96e0

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.13e-1

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

GenotypeQuality
all individuals: 32
bin: 2.5e0
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GenotypeQuality
all individuals: 169
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 45
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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: 12288
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3988
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14976
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.031353135313531e-4
allele num: 9696
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.062118775225321e-4
allele num: 65906
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

QD
type: SiteQuality
SIO_000300: 1.383e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.96e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.102384e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.13e-1

GenotypeQuality
all individuals: 4885
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 20882
bin: 6.25e1
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GenotypeQuality
all individuals: 2714
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514921981517952e-5
allele num: 66010
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15204
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 1.482e1

DP
type: SiteQuality
SIO_000300: 2.110619e6

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

MQRankSum
type: SiteQuality
SIO_000300: 1.91e0

FS
type: SiteQuality
SIO_000300: 4.464e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2714
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GenotypeQuality
all individuals: 7730
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514921981517952e-5
allele num: 66010
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15204
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 2.110619e6

QD
type: SiteQuality
SIO_000300: 1.482e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

FS
type: SiteQuality
SIO_000300: 4.464e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.141552511415525e-3
allele num: 876
num of homozygotes: 0

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

East Asian
type: Population
allele count: 44
allele frequency: 5.136586504786365e-3
allele num: 8566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66054
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15294
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.133e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.919e1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

QD
type: SiteQuality
SIO_000300: 1.191e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.35e0

DP
type: SiteQuality
SIO_000300: 2.116797e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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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: 1814
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.026272577996716e-4
allele num: 9744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 6
allele frequency: 3.868471953578336e-4
allele num: 15510
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.75e-1

DP
type: SiteQuality
SIO_000300: 2.120643e6

FS
type: SiteQuality
SIO_000300: 4.343e0

MQRankSum
type: SiteQuality
SIO_000300: 4.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.659e0

QD
type: SiteQuality
SIO_000300: 1.24e1

GenotypeQuality
all individuals: 231
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12258
bin: 9.75e1
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
all individuals: 4898
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GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511441613010489e-5
allele num: 66162
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15510
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.659e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.59e-1

DP
type: SiteQuality
SIO_000300: 2.120643e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 4.343e0

QD
type: SiteQuality
SIO_000300: 1.24e1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7854
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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
all individuals: 12250
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.334726973267453e-5
allele num: 15786
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.19e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.141e0

VQSLOD
type: SiteQuality
SIO_000300: -2.476e0

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.127607e6

GenotypeQuality
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bin: 9.75e1
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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bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15946
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507204437209863e-5
allele num: 66348
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: 894
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.706e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

QD
type: SiteQuality
SIO_000300: 1.428e1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 8.289999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

DP
type: SiteQuality
SIO_000300: 2.131529e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQ
type: SiteQuality
SIO_000300: 5.793e1

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: 105
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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: 9784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503759398496241e-5
allele num: 66500
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16250
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.507e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.387e0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.140238e6

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.736e0

MQ
type: SiteQuality
SIO_000300: 5.874e1

MQRankSum
type: SiteQuality
SIO_000300: -1.363e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.87e-1

QD
type: SiteQuality
SIO_000300: 1.233e1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.150818058801821e-5
allele num: 16258
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: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66492
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.37e-2

MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.56e-1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.45e-1

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

GenotypeQuality
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variant carriers: 2

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

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

East Asian
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allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000210014701029e-5
allele num: 66662
num of homozygotes: 0

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

South Asian
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allele count: 0
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

MQRankSum
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SIO_000300: 1.18e0

VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
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QD
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MQ
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SIO_000300: 5.903e1

FS
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SIO_000300: 1.742e0

ReadPosRankSum
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SIO_000300: 3.49e-1

ClippingRankSum
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SIO_000300: 1.61e-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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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 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: 1
allele frequency: 1.02124183006536e-4
allele num: 9792
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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ReadPosRankSum
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BaseQRankSum
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DP
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MQRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
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QD
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
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SIO_000300: 4.0e-4

GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

South Asian
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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: 6
allele frequency: 8.996311512279965e-5
allele num: 66694
num of homozygotes: 0

VQSLOD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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DP
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FS
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QD
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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: 66694
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: 1.021033285685113e-4
allele num: 9794
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.297e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.91e1

InbreedingCoeff
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QD
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ClippingRankSum
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SIO_000300: -3.1e-1

BaseQRankSum
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DP
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e-1

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
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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

African
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allele count: 3
allele frequency: 3.06309985705534e-4
allele num: 9794
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.021033285685113e-4
allele num: 9794
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.998500749625187e-5
allele num: 66700
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Other
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South Asian
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African
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East Asian
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allele num: 8620
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DP
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
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BaseQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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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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variant carriers: 0

European (Non-Finnish)
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allele num: 66704
num of homozygotes: 0

Other
type: Population
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Latino
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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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South Asian
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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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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Latino
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allele num: 11570
num of homozygotes: 0

European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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African
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Other
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DP
type: SiteQuality
SIO_000300: 2.148833e6

MQRankSum
type: SiteQuality
SIO_000300: -8.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.684e-1

FS
type: SiteQuality
SIO_000300: 3.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e0

QD
type: SiteQuality
SIO_000300: 1.706e1

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23427
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 44
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4911
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12238
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2712
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7986
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.256e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.444e1

MQRankSum
type: SiteQuality
SIO_000300: 8.29e-1

DP
type: SiteQuality
SIO_000300: 2.14889e6

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.094e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

VQSLOD
type: SiteQuality
SIO_000300: 5.570000000000001e-1

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23426
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7988
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4912
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12237
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 2
allele frequency: 2.041649652919559e-4
allele num: 9796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.28e-1

DP
type: SiteQuality
SIO_000300: 2.148904e6

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: 8.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.522e1