4-88104550-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88104550
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88104550
    reference: chr 4
allele count: 3
allele frequency: 2.670036846508482e-5
allele num: 112358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-12783T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.766-9T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-9T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.766-9T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-4778T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-4778T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.538-9T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-4778T>C
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24455
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2608
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

4-88104552-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88104552
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88104552
    reference: chr 4
allele count: 1
allele frequency: 8.981498113885396e-6
allele num: 111340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-12785C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-11C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.766-11C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.538-11C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.766-11C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-4780C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-4780C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-4780C>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2604
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33687
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11422
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

4-88104555-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88104555
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88104555
    reference: chr 4
allele count: 1
allele frequency: 9.13191971216189e-6
allele num: 109506
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-12788A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-4783A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-4783A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-4783A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.766-14A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-14A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.538-14A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.766-14A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30884
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

4-88104564-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88104564
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88104564
    reference: chr 4
allele count: 2
allele frequency: 1.902804734178179e-5
allele num: 105108
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.766-23A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.538-23A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-4792A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-4792A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-23A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-4792A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-12797A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.766-23A>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18523
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2593
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3537
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

4-88104572-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88104572
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88104572
    reference: chr 4
allele count: 1
allele frequency: 9.932853907584728e-6
allele num: 100676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-31T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-4800T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-4800T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-4800T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.538-31T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-12805T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.766-31T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.766-31T>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8942
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2141
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4922
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2099
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

4-88104575-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88104575
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88104575
    reference: chr 4
allele count: 1
allele frequency: 1.013643643440712e-5
allele num: 98654
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-4803A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-34A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.766-34A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-4803A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-4803A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.766-34A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.538-34A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-12808A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19563
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9319
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2638
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4668
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

4-88104577-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88104577
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88104577
    reference: chr 4
allele count: 1
allele frequency: 1.013951979234263e-5
allele num: 98624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-36T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.538-36T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-4805T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-12810T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.766-36T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.766-36T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-4805T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-4805T>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22623
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5084
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19797
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

4-88104583-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88104583
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88104583
    reference: chr 4
allele count: 1
allele frequency: 1.067030879873663e-5
allele num: 93718
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.766-42A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-12816A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.538-42A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-4811A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-4811A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.766-42A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-42A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-4811A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13297
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8254
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5227
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5521
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

4-88104584-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88104584
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88104583
    reference: chr 4
allele count: 1
allele frequency: 1.080403638799455e-5
allele num: 92558
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.538-44delA
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-44delA
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-4813delA
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.766-44delA
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-4813delA
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-12818delA
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-4813delA
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.766-44delA
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20573
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3605
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16601
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: CT
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

4-88106361-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106361
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106361
    reference: chr 4
allele count: 1
allele frequency: 8.934474563550918e-6
allele num: 111926
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.765+42T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.765+42T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1820T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.537+42T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6589T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14594T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6589T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6589T>C
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28873
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2804
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36196
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

4-88106366-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106366
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106366
    reference: chr 4
allele count: 3
allele frequency: 2.677041690462593e-5
allele num: 112064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6594T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6594T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14599T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.537+37T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1825T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6594T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.765+37T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.765+37T>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10864
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2838
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2801
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2529
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

4-88106372-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106372
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106372
    reference: chr 4
allele count: 22
allele frequency: 1.959457052264063e-4
allele num: 112276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.537+31A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.765+31A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14605A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1831A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.765+31A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6600A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6600A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6600A>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10980
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 9.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 971
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2943
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1365
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

4-88106374-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106374
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106374
    reference: chr 4
allele count: 3
allele frequency: 2.671511006625347e-5
allele num: 112296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1833A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14607A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6602A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.765+29A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6602A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6602A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.765+29A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.537+29A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3060
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1364
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9198
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-88106377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106377
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106377
    reference: chr 4
allele count: 3
allele frequency: 2.668184567220463e-5
allele num: 112436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1836C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.537+26C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6605C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6605C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.765+26C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.765+26C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14610C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6605C>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2806
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3208
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

4-88106385-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106385
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106385
    reference: chr 4
allele count: 2
allele frequency: 1.772326887971218e-5
allele num: 112846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.765+18A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14618A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1844A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6613A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6613A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.537+18A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.765+18A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6613A>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9225
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2805
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36817
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

4-88106391-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106391
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106391
    reference: chr 4
allele count: 1
allele frequency: 8.831269759966088e-6
allele num: 113234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6619A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14624A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1850A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.765+12A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6619A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6619A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.765+12A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.537+12A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2832
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3578
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

4-88106407-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106407
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106407
    reference: chr 4
allele count: 1
allele frequency: 8.640801866413203e-6
allele num: 115730
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14640C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.533C>T
  hgvsp: ENSP00000426451.1:p.Ala178Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6635C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6635C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.761C>T
  hgvsp: ENSP00000273963.5:p.Ala254Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1866C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6635C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.761C>T
  hgvsp: ENSP00000424131.1:p.Ala254Val
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2813
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2822
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala254Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

4-88106419-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106419
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106419
    reference: chr 4
allele count: 1
allele frequency: 8.500076500688507e-6
allele num: 117646
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.749A>G
  hgvsp: ENSP00000273963.5:p.Asp250Gly
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6647A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6647A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.521A>G
  hgvsp: ENSP00000426451.1:p.Asp174Gly
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6647A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14652A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.749A>G
  hgvsp: ENSP00000424131.1:p.Asp250Gly
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1878A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2863
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9416
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp250Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

4-88106428-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106428
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106428
    reference: chr 4
allele count: 1
allele frequency: 8.395036854211791e-6
allele num: 119118
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6656A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.740A>C
  hgvsp: ENSP00000273963.5:p.Lys247Thr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6656A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.740A>C
  hgvsp: ENSP00000424131.1:p.Lys247Thr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1887A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6656A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.512A>C
  hgvsp: ENSP00000426451.1:p.Lys171Thr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14661A>C
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2885
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1190
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Lys247Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

4-88106446-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106446
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106446
    reference: chr 4
allele count: 1
allele frequency: 8.290911502810618e-6
allele num: 120614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1905A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6674A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6674A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.722A>G
  hgvsp: ENSP00000273963.5:p.Asn241Ser
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.722A>G
  hgvsp: ENSP00000424131.1:p.Asn241Ser
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6674A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.494A>G
  hgvsp: ENSP00000426451.1:p.Asn165Ser
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14679A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9599
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn241Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

4-88106449-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106449
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106449
    reference: chr 4
allele count: 1
allele frequency: 8.28363154406892e-6
allele num: 120720
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.719C>T
  hgvsp: ENSP00000273963.5:p.Ala240Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6677C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1908C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14682C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6677C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6677C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.491C>T
  hgvsp: ENSP00000426451.1:p.Ala164Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.719C>T
  hgvsp: ENSP00000424131.1:p.Ala240Val
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40963
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala240Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

4-88106472-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106472
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106472
    reference: chr 4
allele count: 5
allele frequency: 4.121264074116813e-5
allele num: 121322
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.696T>C
  hgvsp: ENST00000273963.5:c.696T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.696T>C
  hgvsp: ENST00000512111.1:c.696T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6700T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6700T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1931T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.468T>C
  hgvsp: ENST00000498875.2:c.468T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6700T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14705T>C
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2916
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn232Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

4-88106474-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106474
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106474
    reference: chr 4
allele count: 8
allele frequency: 6.593153010598494e-5
allele num: 121338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6702A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6702A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14707A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6702A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.694A>G
  hgvsp: ENSP00000273963.5:p.Asn232Asp
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.694A>G
  hgvsp: ENSP00000424131.1:p.Asn232Asp
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.466A>G
  hgvsp: ENSP00000426451.1:p.Asn156Asp
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1933A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2962
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn232Asp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

4-88106483-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106483
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106483
    reference: chr 4
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.685C>G
  hgvsp: ENSP00000273963.5:p.Gln229Glu
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6711C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.457C>G
  hgvsp: ENSP00000426451.1:p.Gln153Glu
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6711C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1942C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14716C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.685C>G
  hgvsp: ENSP00000424131.1:p.Gln229Glu
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6711C>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1423
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln229Glu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

4-88106497-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106497
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106497
    reference: chr 4
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.671T>C
  hgvsp: ENSP00000424131.1:p.Ile224Thr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14730T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.443T>C
  hgvsp: ENSP00000426451.1:p.Ile148Thr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6725T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6725T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6725T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.671T>C
  hgvsp: ENSP00000273963.5:p.Ile224Thr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1956T>C
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2919
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2963
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile224Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

4-88106507-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106507
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106507
    reference: chr 4
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6735G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14740G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.433G>A
  hgvsp: ENSP00000426451.1:p.Asp145Asn
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6735G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.661G>A
  hgvsp: ENSP00000424131.1:p.Asp221Asn
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1966G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.661G>A
  hgvsp: ENSP00000273963.5:p.Asp221Asn
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6735G>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41484
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp221Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

4-88106510-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106510
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106510
    reference: chr 4
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14743A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6738A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6738A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1969A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.430A>G
  hgvsp: ENSP00000426451.1:p.Ser144Gly
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.658A>G
  hgvsp: ENSP00000273963.5:p.Ser220Gly
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.658A>G
  hgvsp: ENSP00000424131.1:p.Ser220Gly
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6738A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser220Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum

4-88106526-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106526
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106526
    reference: chr 4
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14759T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6754T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6754T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.414T>C
  hgvsp: ENST00000498875.2:c.414T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.642T>C
  hgvsp: ENST00000512111.1:c.642T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.642T>C
  hgvsp: ENST00000273963.5:c.642T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1985T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6754T>C
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30342
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 7.75e1
  variant carriers: 0
hgvs: p.His214His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

4-88106527-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106527
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106527
    reference: chr 4
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6755A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6755A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14760A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.641A>G
  hgvsp: ENSP00000273963.5:p.His214Arg
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.641A>G
  hgvsp: ENSP00000424131.1:p.His214Arg
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1986A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.413A>G
  hgvsp: ENSP00000426451.1:p.His138Arg
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6755A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His214Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

4-88106528-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106528
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106528
    reference: chr 4
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6756C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1987C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.412C>G
  hgvsp: ENSP00000426451.1:p.His138Asp
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.640C>G
  hgvsp: ENSP00000273963.5:p.His214Asp
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14761C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6756C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.640C>G
  hgvsp: ENSP00000424131.1:p.His214Asp
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6756C>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41492
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His214Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

4-88106529-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106529
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106529
    reference: chr 4
allele count: 6
allele frequency: 4.942257952916756e-5
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.411C>G
  hgvsp: ENST00000498875.2:c.411C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6757C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14762C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6757C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.639C>G
  hgvsp: ENST00000273963.5:c.639C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1988C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.639C>G
  hgvsp: ENST00000512111.1:c.639C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6757C>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2914
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41491
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9725
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu213Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

4-88106531-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106531
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106531
    reference: chr 4
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6759C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.409C>G
  hgvsp: ENSP00000426451.1:p.Leu137Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6759C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1990C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.637C>G
  hgvsp: ENSP00000273963.5:p.Leu213Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14764C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6759C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.637C>G
  hgvsp: ENSP00000424131.1:p.Leu213Val
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2914
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41492
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu213Val
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

4-88106538-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106538
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106538
    reference: chr 4
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.630G>A
  hgvsp: ENST00000273963.5:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.630G>A
  hgvsp: ENST00000512111.1:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.402G>A
  hgvsp: ENST00000498875.2:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6766G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1997G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14771G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6766G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6766G>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro210Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-88106539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106539
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106539
    reference: chr 4
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-1998C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.629C>T
  hgvsp: ENSP00000273963.5:p.Pro210Leu
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.629C>T
  hgvsp: ENSP00000424131.1:p.Pro210Leu
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.401C>T
  hgvsp: ENSP00000426451.1:p.Pro134Leu
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6767C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6767C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14772C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6767C>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41499
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2968
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro210Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

4-88106550-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106550
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106550
    reference: chr 4
allele count: 7
allele frequency: 5.766157597324503e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6778A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6778A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14783A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.618A>T
  hgvsp: ENST00000273963.5:c.618A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.390A>T
  hgvsp: ENST00000498875.2:c.390A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6778A>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.618A>T
  hgvsp: ENST00000512111.1:c.618A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2009A>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41484
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val206Val
num of homozygotes: 1
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

4-88106564-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106564
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106564
    reference: chr 4
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.376T>C
  hgvsp: ENSP00000426451.1:p.Cys126Arg
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.604T>C
  hgvsp: ENSP00000273963.5:p.Cys202Arg
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2023T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6792T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6792T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14797T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6792T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.604T>C
  hgvsp: ENSP00000424131.1:p.Cys202Arg
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2962
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys202Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

4-88106584-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106584
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106584
    reference: chr 4
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.584A>C
  hgvsp: ENSP00000273963.5:p.His195Pro
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.356A>C
  hgvsp: ENSP00000426451.1:p.His119Pro
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.584A>C
  hgvsp: ENSP00000424131.1:p.His195Pro
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6812A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2043A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6812A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14817A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6812A>C
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41407
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His195Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

4-88106598-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106598
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106598
    reference: chr 4
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.342G>A
  hgvsp: ENST00000498875.2:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.570G>A
  hgvsp: ENST00000512111.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6826G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6826G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.570G>A
  hgvsp: ENST00000273963.5:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14831G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2057G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6826G>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41312
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln190Gln
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-88106603-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106603
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106603
    reference: chr 4
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.337G>T
  hgvsp: ENSP00000426451.1:p.Asp113Tyr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6831G>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14836G>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6831G>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.565G>T
  hgvsp: ENSP00000424131.1:p.Asp189Tyr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.565G>T
  hgvsp: ENSP00000273963.5:p.Asp189Tyr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2062G>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6831G>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9698
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp189Tyr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

4-88106604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106604
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106604
    reference: chr 4
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.564G>A
  hgvsp: ENST00000273963.5:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.336G>A
  hgvsp: ENST00000498875.2:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6832G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14837G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.564G>A
  hgvsp: ENST00000512111.1:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2063G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6832G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6832G>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2910
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41304
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala188Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-88106608-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106608
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106608
    reference: chr 4
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14841T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6836T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.560T>C
  hgvsp: ENSP00000273963.5:p.Met187Thr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6836T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2067T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6836T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.332T>C
  hgvsp: ENSP00000426451.1:p.Met111Thr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.560T>C
  hgvsp: ENSP00000424131.1:p.Met187Thr
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41325
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met187Thr
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

4-88106609-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106609
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106609
    reference: chr 4
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6837A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.559A>G
  hgvsp: ENSP00000273963.5:p.Met187Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6837A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14842A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6837A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2068A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.331A>G
  hgvsp: ENSP00000426451.1:p.Met111Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.559A>G
  hgvsp: ENSP00000424131.1:p.Met187Val
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2958
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Met187Val
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

4-88106610-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106610
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106610
    reference: chr 4
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14843C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6838C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.330C>T
  hgvsp: ENST00000498875.2:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2069C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.558C>T
  hgvsp: ENST00000512111.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.558C>T
  hgvsp: ENST00000273963.5:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6838C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6838C>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41309
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9706
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp186Asp
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

4-88106611-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106611
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106611
    reference: chr 4
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6839A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.557A>G
  hgvsp: ENSP00000424131.1:p.Asp186Gly
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.557A>G
  hgvsp: ENSP00000273963.5:p.Asp186Gly
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6839A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14844A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6839A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2070A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.329A>G
  hgvsp: ENSP00000426451.1:p.Asp110Gly
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9706
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp186Gly
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

4-88106613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106613
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106613
    reference: chr 4
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6841G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6841G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.555G>A
  hgvsp: ENSP00000273963.5:p.Met185Ile
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6841G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.555G>A
  hgvsp: ENSP00000424131.1:p.Met185Ile
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14846G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.327G>A
  hgvsp: ENSP00000426451.1:p.Met109Ile
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2072G>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Met185Ile
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-88106616-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106616
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106616
    reference: chr 4
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6844A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6844A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6844A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.552A>G
  hgvsp: ENST00000273963.5:c.552A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14849A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.324A>G
  hgvsp: ENST00000498875.2:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.552A>G
  hgvsp: ENST00000512111.1:c.552A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2075A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9706
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu184Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

4-88106627-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106627
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106627
    reference: chr 4
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2086C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14860C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6855C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.313C>A
  hgvsp: ENST00000498875.2:c.313C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6855C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.541C>A
  hgvsp: ENST00000512111.1:c.541C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6855C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.541C>A
  hgvsp: ENST00000273963.5:c.541C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41311
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg181Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

4-88106634-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106634
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106634
    reference: chr 4
allele count: 4
allele frequency: 3.295707341188102e-5
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.534T>A
  hgvsp: ENSP00000273963.5:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.534T>A
  hgvsp: ENSP00000424131.1:p.Ser178Arg
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.306T>A
  hgvsp: ENSP00000426451.1:p.Ser102Arg
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6862T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2093T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6862T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14867T>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6862T>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9700
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser178Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

4-88106656-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106656
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106656
    reference: chr 4
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6884C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.512C>A
  hgvsp: ENSP00000273963.5:p.Ala171Glu
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6884C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.284C>A
  hgvsp: ENSP00000426451.1:p.Ala95Glu
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14889C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2115C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6884C>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.512C>A
  hgvsp: ENSP00000424131.1:p.Ala171Glu
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2958
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala171Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

4-88106657-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106657
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106657
    reference: chr 4
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6885G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.511G>A
  hgvsp: ENSP00000424131.1:p.Ala171Thr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14890G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6885G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.511G>A
  hgvsp: ENSP00000273963.5:p.Ala171Thr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2116G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6885G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.283G>A
  hgvsp: ENSP00000426451.1:p.Ala95Thr
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala171Thr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

4-88106661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106661
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106661
    reference: chr 4
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.507C>T
  hgvsp: ENST00000273963.5:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.279C>T
  hgvsp: ENST00000498875.2:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6889C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.507C>T
  hgvsp: ENST00000512111.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6889C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6889C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2120C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14894C>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9697
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys169Cys
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

4-88106672-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106672
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106672
    reference: chr 4
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2131C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.496C>G
  hgvsp: ENSP00000424131.1:p.Pro166Ala
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6900C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6900C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.496C>G
  hgvsp: ENSP00000273963.5:p.Pro166Ala
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14905C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.268C>G
  hgvsp: ENSP00000426451.1:p.Pro90Ala
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6900C>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2900
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro166Ala
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum

4-88106688-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106688
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106688
    reference: chr 4
allele count: 4
allele frequency: 3.295435821387378e-5
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14921G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.480G>A
  hgvsp: ENSP00000424131.1:p.Met160Ile
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6916G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.480G>A
  hgvsp: ENSP00000273963.5:p.Met160Ile
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6916G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2147G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6916G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.252G>A
  hgvsp: ENSP00000426451.1:p.Met84Ile
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14856
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2897
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Met160Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS

4-88106703-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106703
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106703
    reference: chr 4
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2162T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6931T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.237T>C
  hgvsp: ENST00000498875.2:c.237T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14936T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.465T>C
  hgvsp: ENST00000512111.1:c.465T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6931T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6931T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.465T>C
  hgvsp: ENST00000273963.5:c.465T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9698
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala155Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

4-88106723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106723
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106723
    reference: chr 4
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14956G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217G>A
  hgvsp: ENSP00000426451.1:p.Val73Ile
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6951G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.445G>A
  hgvsp: ENSP00000273963.5:p.Val149Ile
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6951G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6951G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.445G>A
  hgvsp: ENSP00000424131.1:p.Val149Ile
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2182G>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14930
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2900
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9698
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val149Ile
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: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

4-88106726-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106726
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106726
    reference: chr 4
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-3C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.442C>T
  hgvsp: ENSP00000273963.5:p.Gln148Ter
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6954C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6954C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.442C>T
  hgvsp: ENSP00000424131.1:p.Gln148Ter
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2185C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6954C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14959C>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2957
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9696
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln148Ter
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

4-88106732-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106732
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106732
    reference: chr 4
allele count: 3
allele frequency: 2.47161759132627e-5
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-9A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2191A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6960A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6960A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.436A>C
  hgvsp: ENSP00000424131.1:p.Ile146Leu
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.436A>C
  hgvsp: ENSP00000273963.5:p.Ile146Leu
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6960A>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14965A>C
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile146Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS

http://identifiers.org/exac.variant/4-88106747-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106747
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106747
    reference: chr 4
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6975T>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6975T>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.421T>G
  hgvsp: ENSP00000273963.5:p.Leu141Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-24T>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14980T>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.421T>G
  hgvsp: ENSP00000424131.1:p.Leu141Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2206T>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6975T>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41505
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu141Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

4-88106748-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106748
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106748
    reference: chr 4
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.420C>G
  hgvsp: ENST00000273963.5:c.420C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6976C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.420C>G
  hgvsp: ENST00000512111.1:c.420C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-25C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14981C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6976C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2207C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6976C>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41483
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu140Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/4-88106759-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106759
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106758
    reference: chr 4
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2219delT
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-14993delT
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.408delT
  hgvsp: ENSP00000273963.5:p.Asn136LysfsTer25
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.408delT
  hgvsp: ENSP00000424131.1:p.Asn136LysfsTer25
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-6988delT
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-6988delT
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-37delT
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-6988delT
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 14958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn136LysfsTer25
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: CA
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

4-88106782-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106782
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106782
    reference: chr 4
allele count: 3
allele frequency: 2.472758444470088e-5
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-59G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-7010G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.386G>A
  hgvsp: ENSP00000273963.5:p.Arg129Gln
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-7010G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.386G>A
  hgvsp: ENSP00000424131.1:p.Arg129Gln
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2241G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-7010G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-15015G>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41483
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg129Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

4-88106788-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106788
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106788
    reference: chr 4
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-7016C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.380C>G
  hgvsp: ENSP00000273963.5:p.Ser127Cys
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2247C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-65C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-7016C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-15021C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-7016C>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.380C>G
  hgvsp: ENSP00000424131.1:p.Ser127Cys
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2873
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41486
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2908
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser127Cys
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

4-88106791-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106791
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106791
    reference: chr 4
allele count: 2
allele frequency: 1.649185302460584e-5
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-7019A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.377A>G
  hgvsp: ENSP00000424131.1:p.Tyr126Cys
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2250A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-7019A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.377A>G
  hgvsp: ENSP00000273963.5:p.Tyr126Cys
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-15024A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-68A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-7019A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr126Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

4-88106792-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106792
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106792
    reference: chr 4
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-69T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-7020T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-7020T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.376T>C
  hgvsp: ENSP00000424131.1:p.Tyr126His
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-15025T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2251T>C
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.376T>C
  hgvsp: ENSP00000273963.5:p.Tyr126His
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-7020T>C
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr126His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

4-88106793-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106793
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106793
    reference: chr 4
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-70C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2252C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.375C>T
  hgvsp: ENST00000273963.5:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-7021C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-7021C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-15026C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.375C>T
  hgvsp: ENST00000512111.1:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-7021C>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10773
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41466
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2864
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val125Val
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

4-88106800-TTTACCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106800
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106794
    reference: chr 4
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  consequence: stop_gained
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.362_367delTGGTAA
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: stop_gained
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.362_367delTGGTAA
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-83_217-78delTGGTAA
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 30250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41464
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2847
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu121_Lys123delinsTer
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: TTTACCA
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

4-88106802-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106802
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106802
    reference: chr 4
allele count: 1
allele frequency: 8.251914444151043e-6
allele num: 121184
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.366A>G
  hgvsp: ENST00000512111.1:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-7030A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-7030A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.366A>G
  hgvsp: ENST00000273963.5:c.366A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-79A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-15035A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-7030A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2261A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10691
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1093
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41381
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val122Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

4-88106816-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106816
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106816
    reference: chr 4
allele count: 1
allele frequency: 8.262687356435807e-6
allele num: 121026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-7044A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-93A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.352A>G
  hgvsp: ENSP00000273963.5:p.Ile118Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.352A>G
  hgvsp: ENSP00000424131.1:p.Ile118Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-15049A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-7044A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-7044A>G
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2275A>G
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2832
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1338
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile118Val
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

4-88106818-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106818
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106818
    reference: chr 4
allele count: 2
allele frequency: 1.653220473482343e-5
allele num: 120976
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-95C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.350C>T
  hgvsp: ENSP00000273963.5:p.Ala117Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-7046C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2277C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.350C>T
  hgvsp: ENSP00000424131.1:p.Ala117Val
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-7046C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-7046C>T
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-15051C>T
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2821
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala117Val
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-88106819-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106819
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106819
    reference: chr 4
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-7047G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-96G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.349G>A
  hgvsp: ENSP00000273963.5:p.Ala117Thr
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-7047G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-15052G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-7047G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2278G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.349G>A
  hgvsp: ENSP00000424131.1:p.Ala117Thr
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala117Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

4-88106822-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88106822
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 88106822
    reference: chr 4
allele count: 7
allele frequency: 5.78933439195448e-5
allele num: 120912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000424131
  ensembl transcript: ENST00000512111
  gene symbol: KLHL8
  hgvsc: ENST00000512111.1:c.346G>A
  hgvsp: ENSP00000424131.1:p.Asp116Asn
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000408854
  ensembl transcript: ENST00000425278
  gene symbol: KLHL8
  hgvsc: ENST00000425278.2:c.217-2281G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000504029
  gene symbol: KLHL8
  hgvsc: ENST00000504029.1:n.129-7050G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000273963
  ensembl transcript: ENST00000273963
  gene symbol: KLHL8
  hgvsc: ENST00000273963.5:c.346G>A
  hgvsp: ENSP00000273963.5:p.Asp116Asn
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl transcript: ENST00000505388
  gene symbol: KLHL8
  hgvsc: ENST00000505388.1:n.81-15055G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426451
  ensembl transcript: ENST00000498875
  gene symbol: KLHL8
  hgvsc: ENST00000498875.2:c.217-99G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000439514
  ensembl transcript: ENST00000545252
  gene symbol: KLHL8
  hgvsc: ENST00000545252.1:c.-101-7050G>A
  variant of: http://identifiers.org/hgnc/18644
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145332
  ensembl protein: ENSP00000426361
  ensembl transcript: ENST00000506985
  gene symbol: KLHL8
  hgvsc: ENST00000506985.1:c.217-7050G>A
  variant of: http://identifiers.org/hgnc/18644
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10441
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp116Asn
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 5939
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 428
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10129
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35260
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.240694789081886e-4
allele num: 8060
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13866
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.203177552131715e-5
allele num: 62438
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.64e0

DP
type: SiteQuality
SIO_000300: 1.563211e6

QD
type: SiteQuality
SIO_000300: 1.664e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

MQ
type: SiteQuality
SIO_000300: 5.993e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.53e-1

FS
type: SiteQuality
SIO_000300: 2.055e0

MQRankSum
type: SiteQuality
SIO_000300: 6.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.520000000000001e-2

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5780
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 957
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1426
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.614205004035513e-5
allele num: 61950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11076
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
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
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.509e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e0

VQSLOD
type: SiteQuality
SIO_000300: -9.907e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.325e0

QD
type: SiteQuality
SIO_000300: 8.09e0

DP
type: SiteQuality
SIO_000300: 1.535379e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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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: 828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10972
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.082485386447283e-4
allele num: 9238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7792
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61022
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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

VQSLOD
type: SiteQuality
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QD
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7396
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.402402095879691e-5
allele num: 58782
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10692
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.855e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.294874e6

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -4.205e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.375e0

QD
type: SiteQuality
SIO_000300: 6.2e-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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variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11172
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10438
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6290
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6998
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.768534238822864e-5
allele num: 56544
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -9.164e-1

QD
type: SiteQuality
SIO_000300: 1.454e1

MQRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.506e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

DP
type: SiteQuality
SIO_000300: 1.134005e6

MQ
type: SiteQuality
SIO_000300: 5.92e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e0

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: 0

GenotypeQuality
all individuals: 378
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.68429207824908e-5
allele num: 10326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55444
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
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: 774
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.588e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.08e0

DP
type: SiteQuality
SIO_000300: 1.09115e6

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6776
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.300595238095238e-5
allele num: 10752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.41e-1

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

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.812e0

DP
type: SiteQuality
SIO_000300: 1.089295e6

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10050
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.891431813883109e-5
allele num: 52870
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6212
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9646
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

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

Other
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allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52254
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Latino
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allele count: 1
allele frequency: 1.005227181342983e-4
allele num: 9948
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

VQSLOD
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ReadPosRankSum
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SIO_000300: 1.13e0

MQ
type: SiteQuality
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QD
type: SiteQuality
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FS
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.34e-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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East Asian
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allele count: 0
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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Other
type: Population
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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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.656505137677335e-5
allele num: 64426
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9980
num of homozygotes: 0

VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 3.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

QD
type: SiteQuality
SIO_000300: 1.658e1

FS
type: SiteQuality
SIO_000300: 7.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

DP
type: SiteQuality
SIO_000300: 1.591551e6

GenotypeQuality
all individuals: 482
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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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: 2840
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9196
bin: 6.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550916591705698e-5
allele num: 64478
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10170
num of homozygotes: 0

South Asian
type: Population
allele count: 20
allele frequency: 1.976284584980237e-3
allele num: 10120
num of homozygotes: 1

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

FS
type: SiteQuality
SIO_000300: 9.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.23e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.595014e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

QD
type: SiteQuality
SIO_000300: 1.582e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2805
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.652461151949381e-5
allele num: 64482
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: 816
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.804e0

VQSLOD
type: SiteQuality
SIO_000300: 7.24e-1

QD
type: SiteQuality
SIO_000300: 1.487e1

DP
type: SiteQuality
SIO_000300: 1.595237e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

FS
type: SiteQuality
SIO_000300: 7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.98e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 36632
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550147263990079e-5
allele num: 64510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.739432944859976e-4
allele num: 11498
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.576e0

VQSLOD
type: SiteQuality
SIO_000300: 8.79e-1

FS
type: SiteQuality
SIO_000300: 2.886e0

QD
type: SiteQuality
SIO_000300: 1.262e1

DP
type: SiteQuality
SIO_000300: 1.597297e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

GenotypeQuality
all individuals: 187
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 491
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10490
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547795938583457e-5
allele num: 64608
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.790483649892304e-5
allele num: 10214
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 7.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 1.601586e6

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

QD
type: SiteQuality
SIO_000300: 1.256e1

MQ
type: SiteQuality
SIO_000300: 5.915e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.47e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2804
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variant carriers: 0

GenotypeQuality
all individuals: 37021
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10764
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545977366891349e-5
allele num: 64684
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

FS
type: SiteQuality
SIO_000300: 7.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e0

MQRankSum
type: SiteQuality
SIO_000300: -5.95e-1

QD
type: SiteQuality
SIO_000300: 1.259e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

DP
type: SiteQuality
SIO_000300: 1.605317e6

GenotypeQuality
all individuals: 481
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
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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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variant carriers: 0

GenotypeQuality
all individuals: 491
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variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532520076012996e-5
allele num: 65252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12566
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.205e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

DP
type: SiteQuality
SIO_000300: 1.626585e6

FS
type: SiteQuality
SIO_000300: 4.13e0

QD
type: SiteQuality
SIO_000300: 1.127e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e0

MQRankSum
type: SiteQuality
SIO_000300: -6.46e-1

GenotypeQuality
all individuals: 1909
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13916
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65718
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.663703131039814e-5
allele num: 10348
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.643651e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

MQ
type: SiteQuality
SIO_000300: 5.986e1

MQRankSum
type: SiteQuality
SIO_000300: -1.139e0

FS
type: SiteQuality
SIO_000300: 7.361e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.8e-2

QD
type: SiteQuality
SIO_000300: 1.239e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513637877274241e-5
allele num: 66066
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14972
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-2

FS
type: SiteQuality
SIO_000300: 3.055e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.657674e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.200000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.707e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 40933
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GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16028
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505162708088744e-5
allele num: 66438
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.19e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.479e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.995e0

VQSLOD
type: SiteQuality
SIO_000300: -1.009e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.19e0

DP
type: SiteQuality
SIO_000300: 1.674205e6

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 357
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9607
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2893
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2920
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66476
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: 902
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: 0
allele frequency: 0.0e0
allele num: 16096
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.121e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.113e0

DP
type: SiteQuality
SIO_000300: 1.675816e6

MQ
type: SiteQuality
SIO_000300: 5.991e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.039e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
all individuals: 52
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9691
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.320027648176948e-4
allele num: 11574
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.65e-1

FS
type: SiteQuality
SIO_000300: 3.235e0

MQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 1.684568e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 1.426e1

GenotypeQuality
all individuals: 9698
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2916
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41432
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1183
bin: 9.75e1
variant carriers: 8

South Asian
type: Population
allele count: 8
allele frequency: 4.847309743092584e-4
allele num: 16504
num of homozygotes: 0

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

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: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e-1

FS
type: SiteQuality
SIO_000300: 1.112e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.98e0

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.984e1

QD
type: SiteQuality
SIO_000300: 1.309e1

DP
type: SiteQuality
SIO_000300: 1.684366e6

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9704
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variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2960
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2915
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.011e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e-2

FS
type: SiteQuality
SIO_000300: 2.119e0

DP
type: SiteQuality
SIO_000300: 1.684735e6

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

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

GenotypeQuality
all individuals: 9715
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 1422
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variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 496
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41482
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.549e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.34e0

FS
type: SiteQuality
SIO_000300: 1.739e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.664e0

DP
type: SiteQuality
SIO_000300: 1.685178e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
SIO_000300: 4.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

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

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2963
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9721
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 496
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 7.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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: 66726
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 7.869e0

VQSLOD
type: SiteQuality
SIO_000300: -1.75e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.685009e6

QD
type: SiteQuality
SIO_000300: 1.33e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.621e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.352e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2918
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41493
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9721
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 1.498486528606108e-5
allele num: 66734
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: 10404
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: 8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.211e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

QD
type: SiteQuality
SIO_000300: 1.192e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.685013e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.16e-1

GenotypeQuality
all individuals: 1171
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9725
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41493
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2969
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 2.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

FS
type: SiteQuality
SIO_000300: 1.428e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.1e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

DP
type: SiteQuality
SIO_000300: 1.685073e6

QD
type: SiteQuality
SIO_000300: 1.403e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

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

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

GenotypeQuality
all individuals: 1169
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2969
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41491
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9725
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 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: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 5.517e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.572e0

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.752e-1

QD
type: SiteQuality
SIO_000300: 1.111e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 1.685009e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.49e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

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

East Asian
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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

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

DP
type: SiteQuality
SIO_000300: 1.684984e6

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
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FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.101e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

European (Finnish)
type: Population
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
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.933210076265311e-4
allele num: 8654
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 1.39e1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 1.685345e6

FS
type: SiteQuality
SIO_000300: 5.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 1.286e1

VQSLOD
type: SiteQuality
SIO_000300: 4.66e0

DP
type: SiteQuality
SIO_000300: 1.684865e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 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: 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

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

African
type: Population
allele count: 3
allele frequency: 2.883506343713956e-4
allele num: 10404
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.21e-1

DP
type: SiteQuality
SIO_000300: 1.684967e6

QD
type: SiteQuality
SIO_000300: 1.52e1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

FS
type: SiteQuality
SIO_000300: 3.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

GenotypeQuality
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bin: 7.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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

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

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

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

FS
type: SiteQuality
SIO_000300: 2.368e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.011e0

MQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.03e-1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.684666e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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: 0
allele frequency: 0.0e0
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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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

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

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

Other
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 908
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

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

FS
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
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DP
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VQSLOD
type: SiteQuality
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BaseQRankSum
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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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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
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num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.622e0

MQRankSum
type: SiteQuality
SIO_000300: 9.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.55e-2

MQ
type: SiteQuality
SIO_000300: 5.983e1

QD
type: SiteQuality
SIO_000300: 1.497e1

DP
type: SiteQuality
SIO_000300: 1.683687e6

FS
type: SiteQuality
SIO_000300: 3.478e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.205e0

VQSLOD
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

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

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 1.498845888665727e-5
allele num: 66718
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

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

FS
type: SiteQuality
SIO_000300: 3.246e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.095e0

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -1.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.683661e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
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: 908
num of homozygotes: 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: 11576
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.327e1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

FS
type: SiteQuality
SIO_000300: 5.27e0

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 1.683883e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 1416
bin: 8.25e1
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: 11576
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: 2
allele frequency: 2.997691777331455e-5
allele num: 66718
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: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.02e-1

DP
type: SiteQuality
SIO_000300: 1.683592e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.267e1

MQ
type: SiteQuality
SIO_000300: 5.984e1

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-1

QD
type: SiteQuality
SIO_000300: 1.397e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

DP
type: SiteQuality
SIO_000300: 1.683497e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

VQSLOD
type: SiteQuality
SIO_000300: 2.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
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bin: 2.75e1
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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 16510
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 (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.196e0

FS
type: SiteQuality
SIO_000300: 2.358e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

DP
type: SiteQuality
SIO_000300: 1.68342e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: -8.88e-2

MQ
type: SiteQuality
SIO_000300: 5.984e1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.446e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 0
allele frequency: 0.0e0
allele num: 16510
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: 11574
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.683376e6

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.68343e6

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.936e0

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

East Asian
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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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

Other
type: Population
allele count: 0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.685e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.683159e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 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

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
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: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.073e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.841e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.256e1

DP
type: SiteQuality
SIO_000300: 1.683256e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

GenotypeQuality
all individuals: 41295
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.456022118541559e-4
allele num: 11574
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

QD
type: SiteQuality
SIO_000300: 1.194e1

DP
type: SiteQuality
SIO_000300: 1.683434e6

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

GenotypeQuality
all individuals: 1145
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41343
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
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: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.191e0

FS
type: SiteQuality
SIO_000300: 9.6e-1

DP
type: SiteQuality
SIO_000300: 1.682987e6

QD
type: SiteQuality
SIO_000300: 1.344e1

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.25e1
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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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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: 497
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9701
bin: 6.75e1
variant carriers: 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: 10398
num of homozygotes: 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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 1.162e1

DP
type: SiteQuality
SIO_000300: 1.683007e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.48e-1

FS
type: SiteQuality
SIO_000300: 1.971e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.446e0

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

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2955
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2901
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
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variant carriers: 0

GenotypeQuality
all individuals: 41313
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1143
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 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: 1
allele frequency: 6.056201550387597e-5
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

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: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.682965e6

FS
type: SiteQuality
SIO_000300: 1.128e0

MQRankSum
type: SiteQuality
SIO_000300: -7.99e-1

QD
type: SiteQuality
SIO_000300: 1.304e1

MQ
type: SiteQuality
SIO_000300: 5.904e1

VQSLOD
type: SiteQuality
SIO_000300: 3.2e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.828e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.392e0

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

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9699
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variant carriers: 0

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 497
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variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 3.25e1
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: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
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: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
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: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.69e-1

QD
type: SiteQuality
SIO_000300: 1.197e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e-1

DP
type: SiteQuality
SIO_000300: 1.683002e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 1.899e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.67e-1

GenotypeQuality
all individuals: 41368
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2955
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 9695
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1142
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.622140050843541e-4
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.613e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.17e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.683261e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 1.798e0

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

GenotypeQuality
all individuals: 1411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2959
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
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

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: 66722
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.41e0

FS
type: SiteQuality
SIO_000300: 7.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.294e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
SIO_000300: 1.849e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.080000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.68325e6

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2957
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
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: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.456e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.043e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

QD
type: SiteQuality
SIO_000300: 1.011e1

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

DP
type: SiteQuality
SIO_000300: 1.683418e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.54e-1

FS
type: SiteQuality
SIO_000300: 6.860000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.27e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
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: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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DP
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SIO_000300: 1.683439e6

MQ
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BaseQRankSum
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

African
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allele count: 3
allele frequency: 2.884615384615385e-4
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66724
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East Asian
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allele frequency: 0.0e0
allele num: 8650
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South Asian
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
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MQ
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VQSLOD
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QD
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MQRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

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

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

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

FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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DP
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MQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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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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South Asian
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allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
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Other
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allele frequency: 0.0e0
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MQ
type: SiteQuality
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DP
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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FS
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QD
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10404
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Other
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allele num: 906
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.0197e1

MQ
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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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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Latino
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allele frequency: 0.0e0
allele num: 11556
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.998410842253606e-5
allele num: 66702
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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MQ
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DP
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ReadPosRankSum
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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allele frequency: 9.626492106276473e-5
allele num: 10388
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European (Non-Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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QD
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16508
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East Asian
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African
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European (Finnish)
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Other
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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InbreedingCoeff
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QD
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MQ
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ReadPosRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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Other
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MQ
type: SiteQuality
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FS
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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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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African
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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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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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.012e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.444e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

BaseQRankSum
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SIO_000300: -1.978e0

DP
type: SiteQuality
SIO_000300: 1.678398e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66640
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: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
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: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.994e0

VQSLOD
type: SiteQuality
SIO_000300: 9.26e-1

InbreedingCoeff
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QD
type: SiteQuality
SIO_000300: 1.002e1

MQRankSum
type: SiteQuality
SIO_000300: -5.492e0

DP
type: SiteQuality
SIO_000300: 1.67604e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.486e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.76e-1

MQ
type: SiteQuality
SIO_000300: 4.917e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.48e-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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variant carriers: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10382
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.496e1

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 6.818e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

DP
type: SiteQuality
SIO_000300: 1.674992e6

VQSLOD
type: SiteQuality
SIO_000300: 6.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
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variant carriers: 0

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

Other
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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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European (Non-Finnish)
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allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
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South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
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FS
type: SiteQuality
SIO_000300: 8.048999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.264e-1

DP
type: SiteQuality
SIO_000300: 1.668219e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.142e0

QD
type: SiteQuality
SIO_000300: 1.475e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10352
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.007971123477215e-5
allele num: 66490
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

DP
type: SiteQuality
SIO_000300: 1.667042e6

FS
type: SiteQuality
SIO_000300: 1.405e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.236e1

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.883e1

ReadPosRankSum
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VQSLOD
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FS
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
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DP
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BaseQRankSum
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QD
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ClippingRankSum
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