19-10672566-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10672566
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10672566
    reference: chr 19
allele count: 5
allele frequency: 4.1583499667332e-5
allele num: 120240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.215-45G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.402-45G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*38-45G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*208-45G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.356-45G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.375-45G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.390-45G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*208-45G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-45G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1064-45G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12775
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

19-10672567-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10672567
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10672567
    reference: chr 19
allele count: 5
allele frequency: 4.15973377703827e-5
allele num: 120200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-46C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.215-46C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.402-46C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1064-46C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*208-46C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*38-46C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.356-46C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.390-46C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*208-46C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.375-46C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12774
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2172
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum

19-10672572-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10672572
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10672571
    reference: chr 19
allele count: 2
allele frequency: 1.66472448809722e-5
allele num: 120140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.215-52delG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*208-52delG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.390-52delG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.402-52delG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.375-52delG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-52delG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*208-52delG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.356-52delG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1064-52delG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*38-52delG
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12773
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: TC
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/19-10672573-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10672573
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10672573
    reference: chr 19
allele count: 14
allele frequency: 1.166122476177784e-4
allele num: 120056
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.356-52G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*208-52G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.375-52G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1064-52G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-52G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.390-52G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*208-52G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.215-52G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.402-52G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*38-52G>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12772
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

19-10672573-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10672573
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10672573
    reference: chr 19
allele count: 3
allele frequency: 2.498833877523822e-5
allele num: 120056
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*208-52G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.390-52G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.356-52G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*208-52G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-52G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.402-52G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.375-52G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.215-52G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1064-52G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*38-52G>C
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12772
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

19-10672573-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10672573
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10672573
    reference: chr 19
allele count: 2
allele frequency: 1.665889251682548e-5
allele num: 120056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*208-52G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.375-52G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1064-52G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.390-52G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-52G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.356-52G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.402-52G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.215-52G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*38-52G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*208-52G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12772
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

19-10673357-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673357
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673357
    reference: chr 19
allele count: 1
allele frequency: 8.327365388138501e-6
allele num: 120086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*207+48G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*207+48G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.389+48G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.214+48G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-836G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.401+48G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.355+48G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*37+48G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.374+48G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1063+48G>C
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7055
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2873
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1756
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-10673373-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673373
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673373
    reference: chr 19
allele count: 6
allele frequency: 4.986287708800798e-5
allele num: 120330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.214+32G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.401+32G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1063+32G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*207+32G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-852G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.355+32G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*207+32G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*37+32G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.389+32G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.374+32G>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7053
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35735
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

19-10673377-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673377
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673377
    reference: chr 19
allele count: 4
allele frequency: 3.319391887406227e-5
allele num: 120504
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*37+28C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*207+28C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*207+28C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.355+28C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.214+28C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-856C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.389+28C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.374+28C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.401+28C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1063+28C>G
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3012
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-10673381-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673381
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673380
    reference: chr 19
allele count: 1
allele frequency: 8.2936619835122e-6
allele num: 120574
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.355+23delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*207+23delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*207+23delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-861delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.374+23delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1063+23delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.214+23delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.389+23delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.401+23delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*37+23delC
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1683
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3110
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: TG
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

19-10673385-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673385
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673385
    reference: chr 19
allele count: 40
allele frequency: 3.31356241094801e-4
allele num: 120716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*207+20C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.355+20C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.389+20C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-864C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*37+20C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.401+20C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.214+20C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1063+20C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.374+20C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*207+20C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 9.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

19-10673387-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673387
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673387
    reference: chr 19
allele count: 1
allele frequency: 8.279242283746192e-6
allele num: 120784
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1063+18A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.389+18A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*207+18A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.355+18A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-866A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*37+18A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.214+18A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.401+18A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*207+18A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.374+18A>G
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

19-10673399-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673399
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673399
    reference: chr 19
allele count: 69
allele frequency: 5.696547396925515e-4
allele num: 121126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1063+6G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.389+6G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*37+6G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.355+6G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*207+6G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.214+6G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.401+6G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*207+6G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.374+6G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-878G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 9.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6345
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7062
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4965
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: c.401+6G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-10673404-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673404
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673404
    reference: chr 19
allele count: 2
allele frequency: 1.650083329208125e-5
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.401+1G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-883G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.214+1G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.374+1G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.389+1G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*37+1G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*207+1G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*207+1G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.355+1G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1063+1G>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 7.75e1
  variant carriers: 0
hgvs: c.401+1G>T
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

19-10673413-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673413
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673414
    reference: chr 19
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.365dupA
  hgvsp: ENSP00000445789.1:p.Lys123GlufsTer7
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.392dupA
  hgvsp: ENSP00000320917.6:p.Lys132GlufsTer7
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.380dupA
  hgvsp: ENSP00000355366.5:p.Lys128GlufsTer7
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*198dupA
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*198dupA
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.346dupA
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*28dupA
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1054dupA
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.205dupA
  hgvsp: ENSP00000438000.1:p.Lys70GlufsTer7
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-893dupA
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys132GlufsTer7
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS

19-10673433-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673433
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673432
    reference: chr 19
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.326delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1034delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*178delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.345delC
  hgvsp: ENSP00000445789.1:p.Tyr115Ter
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.372delC
  hgvsp: ENSP00000320917.6:p.Tyr124Ter
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*8delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*178delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.360delC
  hgvsp: ENSP00000355366.5:p.Tyr120Ter
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-913delC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.185delC
  hgvsp: ENSP00000438000.1:p.Tyr62Ter
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr124Ter
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: CG
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

19-10673434-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673434
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673434
    reference: chr 19
allele count: 6
allele frequency: 4.943479550472926e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.185C>T
  hgvsp: ENST00000543682.1:c.185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.360C>T
  hgvsp: ENST00000361821.5:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1034C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-913C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.345C>T
  hgvsp: ENST00000539027.1:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.326C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*8C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.372C>T
  hgvsp: ENST00000312962.6:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*178C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*178C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9639
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr124Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

19-10673440-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673440
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673440
    reference: chr 19
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*172G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*172G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.366G>A
  hgvsp: ENST00000312962.6:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.320G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.339G>A
  hgvsp: ENST00000539027.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.354G>A
  hgvsp: ENST00000361821.5:c.354G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.179G>A
  hgvsp: ENST00000543682.1:c.179G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.*2G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1028G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-919G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35704
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Lys122Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-10673450-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673450
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673450
    reference: chr 19
allele count: 4
allele frequency: 3.29489291598023e-5
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*162T>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1018T>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.310T>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.331T>C
  hgvsp: ENSP00000442213.1:p.Cys111Arg
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-929T>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*162T>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.329T>C
  hgvsp: ENSP00000445789.1:p.Met110Thr
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.344T>C
  hgvsp: ENSP00000355366.5:p.Met115Thr
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.169T>C
  hgvsp: ENSP00000438000.1:p.Met57Thr
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.356T>C
  hgvsp: ENSP00000320917.6:p.Met119Thr
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9661
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met119Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-10673452-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673452
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673452
    reference: chr 19
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.354C>T
  hgvsp: ENST00000312962.6:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.342C>T
  hgvsp: ENST00000361821.5:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-931C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*160C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.327C>T
  hgvsp: ENST00000539027.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*160C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.167C>T
  hgvsp: ENST00000543682.1:c.167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1016C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.329C>T
  hgvsp: ENSP00000442213.1:p.Pro110Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.308C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro110Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

19-10673453-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673453
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673453
    reference: chr 19
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.166C>G
  hgvsp: ENSP00000438000.1:p.Pro56Arg
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1015C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.326C>G
  hgvsp: ENSP00000445789.1:p.Pro109Arg
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.341C>G
  hgvsp: ENSP00000355366.5:p.Pro114Arg
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.353C>G
  hgvsp: ENSP00000320917.6:p.Pro118Arg
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-932C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*159C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.328C>G
  hgvsp: ENSP00000442213.1:p.Pro110Ala
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.307C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*159C>G
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3210
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro118Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

19-10673456-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673456
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673456
    reference: chr 19
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*156G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.350G>A
  hgvsp: ENSP00000320917.6:p.Arg117Gln
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.323G>A
  hgvsp: ENSP00000445789.1:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.325G>A
  hgvsp: ENSP00000442213.1:p.Gly109Ser
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.304G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.338G>A
  hgvsp: ENSP00000355366.5:p.Arg113Gln
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-935G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.163G>A
  hgvsp: ENSP00000438000.1:p.Arg55Gln
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1012G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*156G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg117Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-10673457-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673457
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673457
    reference: chr 19
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.322C>T
  hgvsp: ENSP00000445789.1:p.Arg108Trp
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.303C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.1011C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.162C>T
  hgvsp: ENSP00000438000.1:p.Arg55Trp
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.349C>T
  hgvsp: ENSP00000320917.6:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*155C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.324C>T
  hgvsp: ENST00000544397.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.337C>T
  hgvsp: ENSP00000355366.5:p.Arg113Trp
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*155C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-936C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg117Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

19-10673475-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673475
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673475
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*137G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.319G>A
  hgvsp: ENSP00000355366.5:p.Glu107Lys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-954G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.306G>A
  hgvsp: ENSP00000442213.1:p.Trp102Ter
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.993G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.331G>A
  hgvsp: ENSP00000320917.6:p.Glu111Lys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.304G>A
  hgvsp: ENSP00000445789.1:p.Glu102Lys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*137G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.144G>A
  hgvsp: ENSP00000438000.1:p.Glu49Lys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.285G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35700
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Trp102Ter
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

19-10673478-AGGCTTCTGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673478
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673469
    reference: chr 19
allele count: 4
allele frequency: 3.295381522795802e-5
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.273_281delCCAGAAGCC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.132_140delCCAGAAGCC
  hgvsp: ENSP00000438000.1:p.Pro45_Ala47del
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.981_989delCCAGAAGCC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.292_300delCCAGAAGCC
  hgvsp: ENSP00000445789.1:p.Pro98_Ala100del
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.307_315delCCAGAAGCC
  hgvsp: ENSP00000355366.5:p.Pro103_Ala105del
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.294_302delCCAGAAGCC
  hgvsp: ENSP00000442213.1:p.Gln99_Pro101del
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.319_327delCCAGAAGCC
  hgvsp: ENSP00000320917.6:p.Pro107_Ala109del
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro107_Ala109del
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: AGGCTTCTGG
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-10673480-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673480
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673480
    reference: chr 19
allele count: 4
allele frequency: 3.295435821387378e-5
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.299C>G
  hgvsp: ENSP00000445789.1:p.Ala100Gly
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.326C>G
  hgvsp: ENSP00000320917.6:p.Ala109Gly
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.301C>G
  hgvsp: ENSP00000442213.1:p.Pro101Ala
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.139C>G
  hgvsp: ENSP00000438000.1:p.Ala47Gly
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*132C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.314C>G
  hgvsp: ENSP00000355366.5:p.Ala105Gly
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*132C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.988C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-959C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.280C>G
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala109Gly
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-10673484-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673484
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673484
    reference: chr 19
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.310G>A
  hgvsp: ENSP00000355366.5:p.Glu104Lys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.297G>A
  hgvsp: ENST00000544397.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.276G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*128G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.135G>A
  hgvsp: ENSP00000438000.1:p.Glu46Lys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.984G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-963G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*128G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.322G>A
  hgvsp: ENSP00000320917.6:p.Glu108Lys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.295G>A
  hgvsp: ENSP00000445789.1:p.Glu99Lys
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3208
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu108Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

19-10673486-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673486
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673486
    reference: chr 19
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.982C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.295C>T
  hgvsp: ENSP00000442213.1:p.Gln99Ter
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.320C>T
  hgvsp: ENSP00000320917.6:p.Pro107Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*126C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.293C>T
  hgvsp: ENSP00000445789.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.308C>T
  hgvsp: ENSP00000355366.5:p.Pro103Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-965C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*126C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.133C>T
  hgvsp: ENSP00000438000.1:p.Pro45Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.274C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6945
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln99Ter
num of homozygotes: 1
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

19-10673492-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673492
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673492
    reference: chr 19
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.127A>T
  hgvsp: ENSP00000438000.1:p.Glu43Val
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.314A>T
  hgvsp: ENSP00000320917.6:p.Glu105Val
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.289A>T
  hgvsp: ENSP00000442213.1:p.Arg97Trp
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*120A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.287A>T
  hgvsp: ENSP00000445789.1:p.Glu96Val
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.976A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*120A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.268A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.302A>T
  hgvsp: ENSP00000355366.5:p.Glu101Val
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-971A>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35697
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2654
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu105Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

19-10673493-CCTCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673493
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673489
    reference: chr 19
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.297_300delTGAG
  hgvsp: ENSP00000355366.5:p.Ser99ArgfsTer18
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.282_285delTGAG
  hgvsp: ENSP00000445789.1:p.Ser94ArgfsTer18
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284_287delTGAG
  hgvsp: ENSP00000442213.1:p.Val95GlyfsTer34
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.309_312delTGAG
  hgvsp: ENSP00000320917.6:p.Ser103ArgfsTer18
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*115_*118delTGAG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*115_*118delTGAG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.122_125delTGAG
  hgvsp: ENSP00000438000.1:p.Ser41ArgfsTer18
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.263_266delTGAG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.971_974delTGAG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-976_286-973delTGAG
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser103ArgfsTer18
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: CCTCA
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

19-10673507-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673507
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673507
    reference: chr 19
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.253C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*105C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.112C>T
  hgvsp: ENSP00000438000.1:p.Ser38Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.272C>T
  hgvsp: ENSP00000445789.1:p.Ser91Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.299C>T
  hgvsp: ENSP00000320917.6:p.Ser100Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.287C>T
  hgvsp: ENSP00000355366.5:p.Ser96Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*105C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-986C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.961C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284-10C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser100Leu
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

19-10673509-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673509
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673509
    reference: chr 19
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.285G>C
  hgvsp: ENST00000361821.5:c.285G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.110G>C
  hgvsp: ENST00000543682.1:c.110G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.297G>C
  hgvsp: ENST00000312962.6:c.297G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.251G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.959G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.270G>C
  hgvsp: ENST00000539027.1:c.270G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*103G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284-12G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-988G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*103G>C
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2850
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser99Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

19-10673517-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673517
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673517
    reference: chr 19
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*99-4A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284-20A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.955-4A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.293-4A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-996A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.266-4A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.281-4A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.247-4A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.106-4A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*99-4A>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: c.293-4A>T
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-10673525-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673525
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673525
    reference: chr 19
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*99-12G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.106-12G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.266-12G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.955-12G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284-28G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*99-12G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.247-12G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.281-12G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.293-12G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-1004G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35689
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-10673533-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673533
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673533
    reference: chr 19
allele count: 29
allele frequency: 2.40611984136203e-4
allele num: 120526
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*99-20T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.955-20T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.106-20T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.281-20T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284-36T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*99-20T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-1012T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.266-20T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.247-20T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.293-20T>G
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6141
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5673
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4909
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7026
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8169
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

19-10673537-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673537
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673537
    reference: chr 19
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*99-24C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.955-24C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.281-24C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.293-24C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284-40C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*99-24C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.266-24C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-1016C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.247-24C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.106-24C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3119
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

19-10673545-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673545
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673545
    reference: chr 19
allele count: 17
allele frequency: 1.405981209474659e-4
allele num: 120912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.955-32G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.281-32G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284-48G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.293-32G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*99-32G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-1024G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.106-32G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.247-32G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*99-32G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.266-32G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7026
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

19-10673554-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673554
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673554
    reference: chr 19
allele count: 4
allele frequency: 3.312794010468429e-5
allele num: 120744
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.293-41G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.266-41G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*99-41G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.106-41G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.247-41G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*99-41G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.955-41G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284-57G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-1033G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.281-41G>C
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6869
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6322
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7018
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

19-10673556-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673556
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673556
    reference: chr 19
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284-59A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*99-43A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.955-43A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*99-43A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.247-43A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.281-43A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.293-43A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-1035A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.106-43A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.266-43A>C
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7013
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5092
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2805
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2409
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

19-10673563-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673563
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673563
    reference: chr 19
allele count: 1
allele frequency: 8.319329129299013e-6
allele num: 120202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.281-50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.247-50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*99-50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.293-50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.106-50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*99-50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.955-50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284-66G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-1042G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.266-50G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

19-10673565-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10673565
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10673565
    reference: chr 19
allele count: 2
allele frequency: 1.664835347784104e-5
allele num: 120132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.286-1044C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.284-68C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*99-52C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.247-52C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*99-52C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.955-52C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.106-52C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.266-52C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.293-52C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.281-52C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6966
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1726
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

19-10675554-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675554
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675554
    reference: chr 19
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+51G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+51G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+51G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+51G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+51G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+51G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+51G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+51G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+1028G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+51G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3086
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

19-10675555-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675555
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675555
    reference: chr 19
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+1027G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+50G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+50G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2341
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

19-10675557-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675557
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675556
    reference: chr 19
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+47delT
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+47delT
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+1024delT
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+47delT
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+47delT
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+47delT
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+47delT
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+47delT
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+47delT
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+47delT
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: GA
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

19-10675560-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675560
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675560
    reference: chr 19
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+45A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+45A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+45A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+45A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+45A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+1022A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+45A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+45A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+45A>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+45A>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21600
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

19-10675564-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675564
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675564
    reference: chr 19
allele count: 16462
allele frequency: 1.356862615805611e-1
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+41G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+41G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+41G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+41G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+41G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+41G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+41G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+41G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+41G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+1018G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16929
  bin: 2.75e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 4.25e1
  variant carriers: 334
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 8.75e1
  variant carriers: 970
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 630
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 8.25e1
  variant carriers: 1025
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 4.75e1
  variant carriers: 466
genotype depth: GenotypeDepth
  all individuals: 12022
  bin: 3.25e1
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 7.25e1
  variant carriers: 1193
genotype depth: GenotypeDepth
  all individuals: 5277
  bin: 3.75e1
  variant carriers: 262
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 954
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 9.25e1
  variant carriers: 931
genotype depth: GenotypeDepth
  all individuals: 5550
  bin: 9.75e1
  variant carriers: 5101
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 7.75e1
  variant carriers: 1105
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.75e1
  variant carriers: 781
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 6.75e1
  variant carriers: 1081
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 1184
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

19-10675572-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675572
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675572
    reference: chr 19
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+33C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+33C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+33C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+33C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+33C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+33C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+33C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+33C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+1010C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+33C>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

19-10675574-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675574
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675574
    reference: chr 19
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+31T>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+31T>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+1008T>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+31T>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+31T>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+31T>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+31T>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+31T>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+31T>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+31T>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22309
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3898
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

19-10675581-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675581
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675581
    reference: chr 19
allele count: 6
allele frequency: 4.943805411818991e-5
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+24C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+24C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+24C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+24C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+24C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+24C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+24C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+24C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+1001C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+24C>G
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3897
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

19-10675590-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675590
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675590
    reference: chr 19
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+15C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+15C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+15C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+15C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+992C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+15C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+15C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+15C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+15C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+15C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15839
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22330
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/19-10675598-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675598
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675598
    reference: chr 19
allele count: 6
allele frequency: 4.94323518265254e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+7G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+7G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+7G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+7G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+7G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+984G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+7G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+7G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+7G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+7G>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
hgvs: c.292+7G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-10675599-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675599
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675599
    reference: chr 19
allele count: 6
allele frequency: 4.94323518265254e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+6G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+6G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+6G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+6G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+6G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+6G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+6G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+6G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+6G>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+983G>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 28959
  bin: 6.25e1
  variant carriers: 0
hgvs: c.292+6G>T
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

19-10675601-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675601
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675601
    reference: chr 19
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+4C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+4C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+4C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+4C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+4C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+981C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+4C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+4C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+4C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+4C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22347
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 8.25e1
  variant carriers: 0
hgvs: c.292+4C>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-10675602-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675602
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675602
    reference: chr 19
allele count: 46
allele frequency: 3.789813640033614e-4
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*98+3C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*98+3C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.292+3C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.954+3C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.265+3C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.280+3C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.246+3C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.283+3C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.285+3C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+980C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6581
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: c.292+3C>T
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

19-10675616-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675616
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675616
    reference: chr 19
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.254A>G
  hgvsp: ENSP00000445789.1:p.Tyr85Cys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.272A>G
  hgvsp: ENSP00000442213.1:p.Tyr91Cys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*87A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.281A>G
  hgvsp: ENSP00000320917.6:p.Tyr94Cys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.269A>G
  hgvsp: ENSP00000355366.5:p.Tyr90Cys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*87A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.235A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.943A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+966A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.274A>G
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr94Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-10675623-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675623
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675623
    reference: chr 19
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.267A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.228A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.265A>G
  hgvsp: ENSP00000442213.1:p.Thr89Ala
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.247A>G
  hgvsp: ENSP00000445789.1:p.Thr83Ala
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.274A>G
  hgvsp: ENSP00000320917.6:p.Thr92Ala
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.936A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.262A>G
  hgvsp: ENSP00000355366.5:p.Thr88Ala
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+959A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*80A>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*80A>G
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr92Ala
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

19-10675624-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675624
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675624
    reference: chr 19
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.273C>G
  hgvsp: ENST00000312962.6:c.273C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.246C>G
  hgvsp: ENST00000539027.1:c.246C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+958C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.935C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.227C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*79C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.266C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.264C>G
  hgvsp: ENST00000544397.1:c.264C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*79C>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.261C>G
  hgvsp: ENST00000361821.5:c.261C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala91Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS

19-10675624-GGCATCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675624
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675618
    reference: chr 19
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*73_*78delAGATGC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.267_272delAGATGC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.260_265delAGATGC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.240_245delAGATGC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+952_105+957delAGATGC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.221_226delAGATGC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.258_263delAGATGC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*73_*78delAGATGC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.255_260delAGATGC
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.929_934delAGATGC
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9883
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys89_Ala91delinsAsn
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: GGCATCT
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

19-10675629-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675629
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675629
    reference: chr 19
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.259G>C
  hgvsp: ENSP00000442213.1:p.Asp87His
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.222G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*74G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.261G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.268G>C
  hgvsp: ENSP00000320917.6:p.Asp90His
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.241G>C
  hgvsp: ENSP00000445789.1:p.Asp81His
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+953G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*74G>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.256G>C
  hgvsp: ENSP00000355366.5:p.Asp86His
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.930G>C
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8946
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29017
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp90His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

19-10675630-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675630
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675630
    reference: chr 19
allele count: 5
allele frequency: 4.118887570844866e-5
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*73A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.260A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.267A>C
  hgvsp: ENSP00000320917.6:p.Lys89Asn
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.929A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*73A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.258A>C
  hgvsp: ENSP00000442213.1:p.Lys86Asn
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.255A>C
  hgvsp: ENSP00000355366.5:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+952A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.221A>C
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.240A>C
  hgvsp: ENSP00000445789.1:p.Lys80Asn
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8946
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys89Asn
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

19-10675635-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675635
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675635
    reference: chr 19
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.250C>A
  hgvsp: ENSP00000355366.5:p.Gln84Lys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.235C>A
  hgvsp: ENSP00000445789.1:p.Gln79Lys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.253C>A
  hgvsp: ENSP00000442213.1:p.Gln85Lys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.262C>A
  hgvsp: ENSP00000320917.6:p.Gln88Lys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*68C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*68C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+947C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.216C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.924C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.255C>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29009
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1914
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln88Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

19-10675644-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675644
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675644
    reference: chr 19
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.226C>T
  hgvsp: ENSP00000445789.1:p.Arg76Cys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+938C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.253C>T
  hgvsp: ENSP00000320917.6:p.Arg85Cys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.241C>T
  hgvsp: ENSP00000355366.5:p.Arg81Cys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*59C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.246C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.207C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.244C>T
  hgvsp: ENSP00000442213.1:p.Arg82Cys
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*59C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.915C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg85Cys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

19-10675648-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675648
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675648
    reference: chr 19
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*55C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.242C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.240C>A
  hgvsp: ENSP00000442213.1:p.Asp80Glu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.222C>A
  hgvsp: ENSP00000445789.1:p.Asp74Glu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.911C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.203C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+934C>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.237C>A
  hgvsp: ENSP00000355366.5:p.Asp79Glu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.249C>A
  hgvsp: ENSP00000320917.6:p.Asp83Glu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*55C>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp83Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ

19-10675650-CCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675650
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675647
    reference: chr 19
allele count: 6
allele frequency: 4.94323518265254e-5
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.198_200delAAG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.237_239delAAG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.906_908delAAG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.217_219delAAG
  hgvsp: ENSP00000445789.1:p.Lys73del
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+929_105+931delAAG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.232_234delAAG
  hgvsp: ENSP00000355366.5:p.Lys78del
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.235_237delAAG
  hgvsp: ENSP00000442213.1:p.Lys79del
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*50_*52delAAG
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.244_246delAAG
  hgvsp: ENSP00000320917.6:p.Lys82del
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*50_*52delAAG
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8942
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys82del
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: CCTT
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

19-10675657-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675657
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675657
    reference: chr 19
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.902G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.240G>A
  hgvsp: ENST00000312962.6:c.240G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.231G>A
  hgvsp: ENST00000544397.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.233G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*46G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*46G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.213G>A
  hgvsp: ENST00000539027.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.194G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.228G>A
  hgvsp: ENST00000361821.5:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+925G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys80Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

19-10675666-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675666
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675666
    reference: chr 19
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.222C>T
  hgvsp: ENST00000544397.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.893C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.185C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+916C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.204C>T
  hgvsp: ENST00000539027.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.231C>T
  hgvsp: ENST00000312962.6:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.224C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*37C>T
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.219C>T
  hgvsp: ENST00000361821.5:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*37C>T
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser77Ser
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

19-10675672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675672
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675672
    reference: chr 19
allele count: 4
allele frequency: 3.29663084327817e-5
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.225G>A
  hgvsp: ENST00000312962.6:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.216G>A
  hgvsp: ENST00000544397.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.218G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*31G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.198G>A
  hgvsp: ENST00000539027.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*31G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.179G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.213G>A
  hgvsp: ENST00000361821.5:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+910G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.887G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr75Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-10675681-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675681
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675681
    reference: chr 19
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+901T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.204T>G
  hgvsp: ENSP00000355366.5:p.Phe68Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*22T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.216T>G
  hgvsp: ENSP00000320917.6:p.Phe72Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.878T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.170T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*22T>G
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.207T>G
  hgvsp: ENSP00000442213.1:p.Phe69Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.189T>G
  hgvsp: ENSP00000445789.1:p.Phe63Leu
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.209T>G
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe72Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

19-10675687-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10675687
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10675687
    reference: chr 19
allele count: 3
allele frequency: 2.474226804123711e-5
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442213
  ensembl transcript: ENST00000544397
  gene symbol: KRI1
  hgvsc: ENST00000544397.1:c.201G>A
  hgvsp: ENST00000544397.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000445789
  ensembl transcript: ENST00000539027
  gene symbol: KRI1
  hgvsc: ENST00000539027.1:c.183G>A
  hgvsp: ENST00000539027.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000478863
  gene symbol: KRI1
  hgvsc: ENST00000478863.1:n.164G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000438000
  ensembl transcript: ENST00000543682
  gene symbol: KRI1
  hgvsc: ENST00000543682.1:c.105+895G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000320917
  ensembl transcript: ENST00000312962
  gene symbol: KRI1
  hgvsc: ENST00000312962.6:c.210G>A
  hgvsp: ENST00000312962.6:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000412919
  ensembl transcript: ENST00000432197
  gene symbol: KRI1
  hgvsc: ENST00000432197.1:c.*16G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000355366
  ensembl transcript: ENST00000361821
  gene symbol: KRI1
  hgvsc: ENST00000361821.5:c.198G>A
  hgvsp: ENST00000361821.5:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000536689
  gene symbol: KRI1
  hgvsc: ENST00000536689.1:n.872G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129347
  ensembl protein: ENSP00000442277
  ensembl transcript: ENST00000546063
  gene symbol: KRI1
  hgvsc: ENST00000546063.1:c.*16G>A
  variant of: http://identifiers.org/hgnc/25769
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129347
  ensembl transcript: ENST00000537964
  gene symbol: KRI1
  hgvsc: ENST00000537964.1:n.203G>A
  variant of: http://identifiers.org/hgnc/25769
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg70Arg
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 675
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49755
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 351
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66338
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: 6614
num of homozygotes: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.322268326417704e-4
allele num: 11568
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.362e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.42e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 4.332398e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 49754
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 981
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.015135982632817e-5
allele num: 66332
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.239081607187422e-5
allele num: 16028
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.849e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 4.332108e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.354e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.224e1

FS
type: SiteQuality
SIO_000300: 2.145e0

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

GenotypeQuality
all individuals: 1047
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 876
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1745
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49759
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 513
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66330
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.252191334835963e-4
allele num: 15972
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

MQ
type: SiteQuality
SIO_000300: 6.031e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.98e-1

DP
type: SiteQuality
SIO_000300: 4.330213e6

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

FS
type: SiteQuality
SIO_000300: 1.862e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

QD
type: SiteQuality
SIO_000300: 2.683e1

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1639
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1044
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49762
bin: 9.75e1
variant carriers: 13

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: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15920
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508250128201261e-5
allele num: 66302
num of homozygotes: 0

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

African
type: Population
allele count: 13
allele frequency: 1.285855588526212e-3
allele num: 10110
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.330205e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

MQ
type: SiteQuality
SIO_000300: 5.937e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.601e0

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

FS
type: SiteQuality
SIO_000300: 1.488e0

QD
type: SiteQuality
SIO_000300: 1.324e1

GenotypeQuality
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49762
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1044
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.967359050445104e-4
allele num: 10110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 66302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15920
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.324e1

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

FS
type: SiteQuality
SIO_000300: 1.488e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

DP
type: SiteQuality
SIO_000300: 4.330205e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.601e0

MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

GenotypeQuality
all individuals: 81
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1044
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 513
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49762
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 966
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508250128201261e-5
allele num: 66302
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15920
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.488e0

DP
type: SiteQuality
SIO_000300: 4.330205e6

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.601e0

QD
type: SiteQuality
SIO_000300: 1.324e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.937e1

GenotypeQuality
all individuals: 621
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35737
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 425
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5954
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2606
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2845
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15642
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.429e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.421e0

DP
type: SiteQuality
SIO_000300: 2.921599e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.34e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

QD
type: SiteQuality
SIO_000300: 1.344e1

MQRankSum
type: SiteQuality
SIO_000300: -1.821e0

FS
type: SiteQuality
SIO_000300: 1.626e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1651
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15808
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.037777911670784e-5
allele num: 66388
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: 8652
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.871e0

FS
type: SiteQuality
SIO_000300: 3.969e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

QD
type: SiteQuality
SIO_000300: 1.386e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

DP
type: SiteQuality
SIO_000300: 2.934939e6

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

GenotypeQuality
all individuals: 280
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

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

GenotypeQuality
all individuals: 7979
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1675
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35736
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66430
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.509725185092233e-4
allele num: 15938
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

FS
type: SiteQuality
SIO_000300: 1.551e0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 1.072e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

DP
type: SiteQuality
SIO_000300: 2.939551e6

MQ
type: SiteQuality
SIO_000300: 5.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2631
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

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

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 8126
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variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 2844
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3012
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35735
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1760
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.256256256256256e-5
allele num: 15984
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66446
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.044e1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

FS
type: SiteQuality
SIO_000300: 3.773e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.196e0

DP
type: SiteQuality
SIO_000300: 2.94287e6

QD
type: SiteQuality
SIO_000300: 1.458e1

GenotypeQuality
all individuals: 2636
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2847
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 242
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variant carriers: 0

GenotypeQuality
all individuals: 3111
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variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 425
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variant carriers: 0

GenotypeQuality
all individuals: 8515
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variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35738
bin: 9.75e1
variant carriers: 40

GenotypeQuality
all individuals: 1760
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 39
allele frequency: 4.507628294036061e-3
allele num: 8652
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.219679064560268e-5
allele num: 16078
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.964e1

FS
type: SiteQuality
SIO_000300: 6.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.549e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

DP
type: SiteQuality
SIO_000300: 2.948455e6

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

GenotypeQuality
all individuals: 2847
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 3114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
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variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35727
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1761
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503488092374308e-5
allele num: 66512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.767e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

VQSLOD
type: SiteQuality
SIO_000300: 4.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 2.945904e6

QD
type: SiteQuality
SIO_000300: 1.277e1

MQ
type: SiteQuality
SIO_000300: 5.932e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

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

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35751
bin: 9.75e1
variant carriers: 69

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 9221
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 2.25e1
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GenotypeQuality
all individuals: 3115
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
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GenotypeQuality
all individuals: 2647
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2849
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3163
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 68
allele frequency: 4.158004158004158e-3
allele num: 16354
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: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.957567e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.07e0

QD
type: SiteQuality
SIO_000300: 1.316e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3181
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 110
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35706
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1708
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9410
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1764
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2850
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001380635092142e-5
allele num: 66636
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.743e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.079e0

DP
type: SiteQuality
SIO_000300: 2.955116e6

QD
type: SiteQuality
SIO_000300: 1.307e1

GenotypeQuality
all individuals: 3120
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1713
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35706
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3201
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9565
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1763
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
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: 66678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.956748e6

MQRankSum
type: SiteQuality
SIO_000300: 9.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.571e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.371e1

FS
type: SiteQuality
SIO_000300: 5.432e0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35705
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

DP
type: SiteQuality
SIO_000300: 2.957766e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.316e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.41e0

QD
type: SiteQuality
SIO_000300: 1.468e1

VQSLOD
type: SiteQuality
SIO_000300: 8.090000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e0

MQ
type: SiteQuality
SIO_000300: 5.893e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.796e0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2852
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3212
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35704
bin: 9.75e1
variant carriers: 6

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2658
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.843936190659235e-4
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 9.18e-1

DP
type: SiteQuality
SIO_000300: 2.958417e6

QD
type: SiteQuality
SIO_000300: 1.219e1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

FS
type: SiteQuality
SIO_000300: 1.105e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.52e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.16e-1

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9654
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2657
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
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: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.31e-1

DP
type: SiteQuality
SIO_000300: 2.957935e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.161e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.011e0

MQRankSum
type: SiteQuality
SIO_000300: -1.852e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.41e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.262e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.879999999999999e-1

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35705
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3120
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.111e0

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.53e-1

DP
type: SiteQuality
SIO_000300: 2.957938e6

QD
type: SiteQuality
SIO_000300: 1.2e1

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.155e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.249e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.508e0

QD
type: SiteQuality
SIO_000300: 1.202e1

FS
type: SiteQuality
SIO_000300: 6.485e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.8e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 2.957492e6

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.283e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.484e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

DP
type: SiteQuality
SIO_000300: 2.957654e6

VQSLOD
type: SiteQuality
SIO_000300: 7.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.590000000000001e-1

GenotypeQuality
all individuals: 1763
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35702
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3120
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variant carriers: 0

GenotypeQuality
all individuals: 9664
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2657
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 6.75e1
variant carriers: 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: 8654
num of homozygotes: 0

South Asian
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allele count: 0
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African
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allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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ClippingRankSum
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MQRankSum
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QD
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DP
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FS
type: SiteQuality
SIO_000300: 2.547e0

InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 1.57e0

MQ
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SIO_000300: 5.941e1

BaseQRankSum
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SIO_000300: 1.5e0

ReadPosRankSum
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SIO_000300: 1.02e0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66730
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South Asian
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allele num: 16510
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

MQRankSum
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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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: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

MQ
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SIO_000300: 5.982e1

MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: 0.0e0

DP
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ClippingRankSum
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SIO_000300: -7.99e-1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 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 count: 4
allele frequency: 4.622140050843541e-4
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.957372e6

FS
type: SiteQuality
SIO_000300: 4.991e0

InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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SIO_000300: 1.64e0

QD
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SIO_000300: 4.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-1

ClippingRankSum
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SIO_000300: 1.2e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
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 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: 6614
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

FS
type: SiteQuality
SIO_000300: 4.757e0

InbreedingCoeff
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SIO_000300: 0.0e0

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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Other
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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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VQSLOD
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

South Asian
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allele frequency: 1.211387038158692e-4
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Latino
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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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DP
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FS
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QD
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MQ
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

Other
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African
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 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 count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
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SIO_000300: -1.134e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.232e0

MQ
type: SiteQuality
SIO_000300: 5.65e1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.697e0

DP
type: SiteQuality
SIO_000300: 2.956286e6

QD
type: SiteQuality
SIO_000300: 1.281e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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
allele num: 906
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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SIO_000300: 2.3e-2

FS
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SIO_000300: 2.161e0

BaseQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.934e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

DP
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SIO_000300: 2.954869e6

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.77e0

DP
type: SiteQuality
SIO_000300: 2.954591e6

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 1.663e0

InbreedingCoeff
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SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.137e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

GenotypeQuality
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variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.939e0

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.765e0

DP
type: SiteQuality
SIO_000300: 2.95258e6

QD
type: SiteQuality
SIO_000300: 1.302e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.566e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 9.74e0

VQSLOD
type: SiteQuality
SIO_000300: 5.51e-1

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.654e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.38e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.539408866995074e-4
allele num: 6496
num of homozygotes: 0

African
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allele count: 6
allele frequency: 5.821851348728896e-4
allele num: 10306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 3.170960045903422e-4
allele num: 66226
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.938195e6

MQ
type: SiteQuality
SIO_000300: 5.851e1

FS
type: SiteQuality
SIO_000300: 2.1282e1

ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.31e-1

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

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

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

East Asian
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allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.518e0

MQ
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.519756838905775e-4
allele num: 6580
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.731301939058172e-4
allele num: 11552
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

African
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allele count: 4
allele frequency: 3.850596842510589e-4
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.353587005564746e-4
allele num: 66490
num of homozygotes: 0

Other
type: Population
allele count: 0
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DP
type: SiteQuality
SIO_000300: 2.919164e6

ReadPosRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
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MQRankSum
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QD
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SIO_000300: 1.356e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66408
num of homozygotes: 0

African
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allele count: 4
allele frequency: 3.852822192255828e-4
allele num: 10382
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.327e0

QD
type: SiteQuality
SIO_000300: 1.353e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.2e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506387081224391e-5
allele num: 66384
num of homozygotes: 0

Other
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allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

MQ
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SIO_000300: 6.0e1

FS
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.07e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66188
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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FS
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DP
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VQSLOD
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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SIO_000300: -2.597e0

ReadPosRankSum
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SIO_000300: 2.39e0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023705853894533e-5
allele num: 66144
num of homozygotes: 0

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

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.603e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.429e1

MQRankSum
type: SiteQuality
SIO_000300: 2.62e0

DP
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.692e0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

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

Other
type: Population
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.36e-1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.865e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

InbreedingCoeff
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
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QD
type: SiteQuality
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FS
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BaseQRankSum
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

East Asian
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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South Asian
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Other
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MQ
type: SiteQuality
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ReadPosRankSum
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DP
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MQRankSum
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FS
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BaseQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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Other
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African
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East Asian
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European (Finnish)
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FS
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InbreedingCoeff
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DP
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QD
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2152
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 6746
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21524
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22375
bin: 9.75e1
variant carriers: 15229

European (Finnish)
type: Population
allele count: 939
allele frequency: 1.419715754460236e-1
allele num: 6614
num of homozygotes: 63

European (Non-Finnish)
type: Population
allele count: 9203
allele frequency: 1.379925628261261e-1
allele num: 66692
num of homozygotes: 680

Other
type: Population
allele count: 136
allele frequency: 1.497797356828194e-1
allele num: 908
num of homozygotes: 11

East Asian
type: Population
allele count: 1393
allele frequency: 1.611522443313281e-1
allele num: 8644
num of homozygotes: 104

African
type: Population
allele count: 821
allele frequency: 7.897268180069257e-2
allele num: 10396
num of homozygotes: 34

Latino
type: Population
allele count: 1308
allele frequency: 1.130509939498704e-1
allele num: 11570
num of homozygotes: 67

South Asian
type: Population
allele count: 2662
allele frequency: 1.613333333333333e-1
allele num: 16500
num of homozygotes: 225

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.982e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.528e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

DP
type: SiteQuality
SIO_000300: 2.862317e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

GenotypeQuality
all individuals: 1223
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1914
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28804
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3898
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variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9916
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8948
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2877
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.61e0

VQSLOD
type: SiteQuality
SIO_000300: -2.482e0

FS
type: SiteQuality
SIO_000300: 1.6637e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 2.078678e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.468e1

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1914
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
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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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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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9915
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 2.693e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-1

DP
type: SiteQuality
SIO_000300: 2.078904e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.218e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.524e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
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: 34
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 28861
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variant carriers: 0

GenotypeQuality
all individuals: 9914
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 2919
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8945
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1915
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variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.993075331994364e-5
allele num: 66718
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.222e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

DP
type: SiteQuality
SIO_000300: 2.079357e6

VQSLOD
type: SiteQuality
SIO_000300: 4.69e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.88e-1

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

GenotypeQuality
all individuals: 28919
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1914
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 9909
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variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2922
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8948
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
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variant carriers: 0

GenotypeQuality
all individuals: 2877
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3894
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
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: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.962e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.21e-1

FS
type: SiteQuality
SIO_000300: 3.247e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

QD
type: SiteQuality
SIO_000300: 1.892e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

DP
type: SiteQuality
SIO_000300: 2.079379e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.951e1

GenotypeQuality
all individuals: 8936
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1914
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 28955
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2923
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 9907
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3890
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.992266650680415e-5
allele num: 66724
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 8652
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.849e0

MQRankSum
type: SiteQuality
SIO_000300: 2.88e-1

DP
type: SiteQuality
SIO_000300: 2.079901e6

QD
type: SiteQuality
SIO_000300: 1.745e1

MQ
type: SiteQuality
SIO_000300: 5.941e1

FS
type: SiteQuality
SIO_000300: 5.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.87e-1

GenotypeQuality
all individuals: 8936
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9906
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2923
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.992266650680415e-5
allele num: 66724
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.079965e6

QD
type: SiteQuality
SIO_000300: 1.768e1

MQRankSum
type: SiteQuality
SIO_000300: 7.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.03e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.416e0

GenotypeQuality
all individuals: 2923
bin: 7.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 8.75e1
variant carriers: 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: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.898e1

MQRankSum
type: SiteQuality
SIO_000300: -3.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

FS
type: SiteQuality
SIO_000300: 3.154e0

VQSLOD
type: SiteQuality
SIO_000300: 6.2e-3

QD
type: SiteQuality
SIO_000300: 1.124e1

DP
type: SiteQuality
SIO_000300: 2.079254e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 42
allele frequency: 2.543912780133252e-3
allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
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: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.081353e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.096e0

MQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 1.204e1

FS
type: SiteQuality
SIO_000300: 1.174e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

GenotypeQuality
all individuals: 1915
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variant carriers: 0

GenotypeQuality
all individuals: 9884
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variant carriers: 2

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.12e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.079016e6

QD
type: SiteQuality
SIO_000300: 1.26e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.32e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
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: 66730
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.289e0

DP
type: SiteQuality
SIO_000300: 2.079007e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.92e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3892
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 29011
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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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
all individuals: 17
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2923
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2872
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8943
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

QD
type: SiteQuality
SIO_000300: 8.890000000000001e0

DP
type: SiteQuality
SIO_000300: 2.079064e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.82e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

FS
type: SiteQuality
SIO_000300: 6.342e0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2872
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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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: 3
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1224
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.82e1

MQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e-1

DP
type: SiteQuality
SIO_000300: 2.079064e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

FS
type: SiteQuality
SIO_000300: 6.342e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

QD
type: SiteQuality
SIO_000300: 8.890000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

GenotypeQuality
all individuals: 2
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.342e1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e0

DP
type: SiteQuality
SIO_000300: 2.079129e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.199e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 3.911e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.167e0

DP
type: SiteQuality
SIO_000300: 2.079274e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.184e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8948
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

DP
type: SiteQuality
SIO_000300: 2.078769e6

BaseQRankSum
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ClippingRankSum
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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QD
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FS
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MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
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SIO_000300: -3.0e-4

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

Latino
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allele frequency: 0.0e0
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Other
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South Asian
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allele frequency: 6.056201550387597e-5
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European (Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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MQ
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InbreedingCoeff
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SIO_000300: 2.0e-4

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

Latino
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South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66726
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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African
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Other
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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SIO_000300: 2.078575e6

ClippingRankSum
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SIO_000300: 6.6e-2

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

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.68e-1

MQ
type: SiteQuality
SIO_000300: 5.877e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6

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

European (Non-Finnish)
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allele frequency: 4.496133325340207e-5
allele num: 66724
num of homozygotes: 0

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

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

African
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allele count: 3
allele frequency: 2.885170225043277e-4
allele num: 10398
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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BaseQRankSum
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SIO_000300: 1.49e0

QD
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SIO_000300: 1.648e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.414e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

DP
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SIO_000300: 2.078765e6

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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BaseQRankSum
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SIO_000300: 6.4e-2

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

Latino
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African
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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InbreedingCoeff
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DP
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BaseQRankSum
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MQ
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8652
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Latino
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African
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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ClippingRankSum
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ReadPosRankSum
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DP
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BaseQRankSum
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FS
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QD
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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