3-183368194-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368194
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368194
    reference: chr 3
allele count: 7
allele frequency: 5.809610756079343e-5
allele num: 120490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.50G>A
  hgvsp: ENSP00000417275.1:p.Arg17His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.50G>A
  hgvsp: ENSP00000416836.2:p.Arg17His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.50G>A
  hgvsp: ENSP00000417347.1:p.Arg17His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.50G>A
  hgvsp: ENSP00000420207.1:p.Arg17His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.50G>A
  hgvsp: ENSP00000408516.1:p.Arg17His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.50G>A
  hgvsp: ENSP00000408567.2:p.Arg17His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.50G>A
  hgvsp: ENSP00000419010.1:p.Arg17His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.50G>A
  hgvsp: ENSP00000395012.1:p.Arg17His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.50G>A
  hgvsp: ENSP00000242810.6:p.Arg17His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.50G>A
  hgvsp: ENSP00000419120.1:p.Arg17His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.50G>A
  hgvsp: ENSP00000418922.1:p.Arg17His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-13052G>A
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg17His
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

3-183368215-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368215
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368215
    reference: chr 3
allele count: 1
allele frequency: 8.276638360563474e-6
allele num: 120822
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.71G>A
  hgvsp: ENSP00000419010.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.71G>A
  hgvsp: ENSP00000417347.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.71G>A
  hgvsp: ENSP00000417275.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.71G>A
  hgvsp: ENSP00000418922.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.71G>A
  hgvsp: ENSP00000419120.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.71G>A
  hgvsp: ENSP00000395012.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.71G>A
  hgvsp: ENSP00000408516.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.71G>A
  hgvsp: ENSP00000420207.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.71G>A
  hgvsp: ENSP00000242810.6:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.71G>A
  hgvsp: ENSP00000408567.2:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.71G>A
  hgvsp: ENSP00000416836.2:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-13031G>A
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg24Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

3-183368216-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368216
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368216
    reference: chr 3
allele count: 34596
allele frequency: 2.857331637456846e-1
allele num: 121078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.72A>T
  hgvsp: ENST00000482138.1:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.72A>T
  hgvsp: ENST00000427201.2:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.72A>T
  hgvsp: ENST00000454652.2:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.72A>T
  hgvsp: ENST00000468001.1:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.72A>T
  hgvsp: ENST00000476808.1:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.72A>T
  hgvsp: ENST00000437402.1:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-13030A>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.72A>T
  hgvsp: ENST00000454495.2:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.72A>T
  hgvsp: ENST00000242810.6:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.72A>T
  hgvsp: ENST00000473045.1:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.72A>T
  hgvsp: ENST00000468101.1:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.72A>T
  hgvsp: ENST00000493074.1:c.72A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 4.75e1
  variant carriers: 1082
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 5.25e1
  variant carriers: 1590
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 3.25e1
  variant carriers: 269
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9825
  bin: 2.75e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 9.25e1
  variant carriers: 1615
genotype depth: GenotypeDepth
  all individuals: 18777
  bin: 2.25e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 764
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 7.75e1
  variant carriers: 2646
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.75e1
  variant carriers: 2079
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 6.25e1
  variant carriers: 2447
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 9.75e1
  variant carriers: 6188
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.75e1
  variant carriers: 412
genotype quality: GenotypeQuality
hgvs: p.Arg24Arg
num of homozygotes: 5494
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS

3-183368239-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368239
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368239
    reference: chr 3
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.95A>G
  hgvsp: ENSP00000420207.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.95A>G
  hgvsp: ENSP00000419010.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.95A>G
  hgvsp: ENSP00000419120.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.95A>G
  hgvsp: ENSP00000418922.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-13007A>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.95A>G
  hgvsp: ENSP00000395012.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.95A>G
  hgvsp: ENSP00000408516.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.95A>G
  hgvsp: ENSP00000242810.6:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.95A>G
  hgvsp: ENSP00000417347.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.95A>G
  hgvsp: ENSP00000417275.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.95A>G
  hgvsp: ENSP00000416836.2:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.95A>G
  hgvsp: ENSP00000408567.2:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys32Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

3-183368249-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368249
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368249
    reference: chr 3
allele count: 2
allele frequency: 1.648994937585542e-5
allele num: 121286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.105A>G
  hgvsp: ENST00000476808.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.105A>G
  hgvsp: ENST00000473045.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.105A>G
  hgvsp: ENST00000437402.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.105A>G
  hgvsp: ENST00000468101.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.105A>G
  hgvsp: ENST00000242810.6:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.105A>G
  hgvsp: ENST00000482138.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.105A>G
  hgvsp: ENST00000493074.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.105A>G
  hgvsp: ENST00000427201.2:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12997A>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.105A>G
  hgvsp: ENST00000454652.2:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.105A>G
  hgvsp: ENST00000468001.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.105A>G
  hgvsp: ENST00000454495.2:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr35Thr
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: A
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-183368255-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368255
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368255
    reference: chr 3
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.111T>C
  hgvsp: ENST00000454495.2:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.111T>C
  hgvsp: ENST00000482138.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.111T>C
  hgvsp: ENST00000437402.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.111T>C
  hgvsp: ENST00000493074.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.111T>C
  hgvsp: ENST00000468001.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.111T>C
  hgvsp: ENST00000427201.2:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.111T>C
  hgvsp: ENST00000473045.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.111T>C
  hgvsp: ENST00000242810.6:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.111T>C
  hgvsp: ENST00000476808.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.111T>C
  hgvsp: ENST00000454652.2:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.111T>C
  hgvsp: ENST00000468101.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12991T>C
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His37His
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

3-183368258-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368258
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368258
    reference: chr 3
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.114G>C
  hgvsp: ENSP00000419010.1:p.Glu38Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12988G>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.114G>C
  hgvsp: ENSP00000420207.1:p.Glu38Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.114G>C
  hgvsp: ENSP00000416836.2:p.Glu38Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.114G>C
  hgvsp: ENSP00000417347.1:p.Glu38Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.114G>C
  hgvsp: ENSP00000242810.6:p.Glu38Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.114G>C
  hgvsp: ENSP00000417275.1:p.Glu38Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.114G>C
  hgvsp: ENSP00000408567.2:p.Glu38Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.114G>C
  hgvsp: ENSP00000418922.1:p.Glu38Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.114G>C
  hgvsp: ENSP00000408516.1:p.Glu38Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.114G>C
  hgvsp: ENSP00000395012.1:p.Glu38Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.114G>C
  hgvsp: ENSP00000419120.1:p.Glu38Asp
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu38Asp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

3-183368264-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368264
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368264
    reference: chr 3
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.120T>C
  hgvsp: ENST00000473045.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.120T>C
  hgvsp: ENST00000242810.6:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12982T>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.120T>C
  hgvsp: ENST00000454652.2:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.120T>C
  hgvsp: ENST00000454495.2:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.120T>C
  hgvsp: ENST00000482138.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.120T>C
  hgvsp: ENST00000476808.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.120T>C
  hgvsp: ENST00000468001.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.120T>C
  hgvsp: ENST00000437402.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.120T>C
  hgvsp: ENST00000493074.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.120T>C
  hgvsp: ENST00000468101.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.120T>C
  hgvsp: ENST00000427201.2:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe40Phe
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-183368266-ACTTCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368266
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368261
    reference: chr 3
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.127_131delTCTTC
  hgvsp: ENSP00000419120.1:p.Ser43ArgfsTer13
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.127_131delTCTTC
  hgvsp: ENSP00000395012.1:p.Ser43ArgfsTer13
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.127_131delTCTTC
  hgvsp: ENSP00000408516.1:p.Ser43ArgfsTer13
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.127_131delTCTTC
  hgvsp: ENSP00000418922.1:p.Ser43ArgfsTer13
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.127_131delTCTTC
  hgvsp: ENSP00000420207.1:p.Ser43ArgfsTer13
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.127_131delTCTTC
  hgvsp: ENSP00000242810.6:p.Ser43ArgfsTer13
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.127_131delTCTTC
  hgvsp: ENSP00000419010.1:p.Ser43ArgfsTer13
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.127_131delTCTTC
  hgvsp: ENSP00000408567.2:p.Ser43ArgfsTer13
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.127_131delTCTTC
  hgvsp: ENSP00000417275.1:p.Ser43ArgfsTer13
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.127_131delTCTTC
  hgvsp: ENSP00000417347.1:p.Ser43ArgfsTer13
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.127_131delTCTTC
  hgvsp: ENSP00000416836.2:p.Ser43ArgfsTer13
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 11620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19338
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser43ArgfsTer13
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: ACTTCT
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

3-183368274-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368274
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368274
    reference: chr 3
allele count: 15
allele frequency: 1.235869887618231e-4
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.130T>A
  hgvsp: ENSP00000417347.1:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.130T>A
  hgvsp: ENSP00000417275.1:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.130T>A
  hgvsp: ENSP00000242810.6:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.130T>A
  hgvsp: ENSP00000419120.1:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12972T>A
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.130T>A
  hgvsp: ENSP00000395012.1:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.130T>A
  hgvsp: ENSP00000418922.1:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.130T>A
  hgvsp: ENSP00000408567.2:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.130T>A
  hgvsp: ENSP00000419010.1:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.130T>A
  hgvsp: ENSP00000408516.1:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.130T>A
  hgvsp: ENSP00000420207.1:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.130T>A
  hgvsp: ENSP00000416836.2:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser44Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/3-183368279-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368279
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368279
    reference: chr 3
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.135A>C
  hgvsp: ENST00000476808.1:c.135A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.135A>C
  hgvsp: ENST00000242810.6:c.135A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.135A>C
  hgvsp: ENST00000493074.1:c.135A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.135A>C
  hgvsp: ENST00000437402.1:c.135A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.135A>C
  hgvsp: ENST00000468101.1:c.135A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.135A>C
  hgvsp: ENST00000454652.2:c.135A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.135A>C
  hgvsp: ENST00000468001.1:c.135A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.135A>C
  hgvsp: ENST00000454495.2:c.135A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.135A>C
  hgvsp: ENST00000482138.1:c.135A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.135A>C
  hgvsp: ENST00000427201.2:c.135A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12967A>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.135A>C
  hgvsp: ENST00000473045.1:c.135A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly45Gly
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

3-183368284-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368284
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368284
    reference: chr 3
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.140C>G
  hgvsp: ENSP00000419120.1:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.140C>G
  hgvsp: ENSP00000408516.1:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.140C>G
  hgvsp: ENSP00000417275.1:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.140C>G
  hgvsp: ENSP00000242810.6:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.140C>G
  hgvsp: ENSP00000418922.1:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.140C>G
  hgvsp: ENSP00000416836.2:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.140C>G
  hgvsp: ENSP00000417347.1:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.140C>G
  hgvsp: ENSP00000419010.1:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.140C>G
  hgvsp: ENSP00000395012.1:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.140C>G
  hgvsp: ENSP00000420207.1:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.140C>G
  hgvsp: ENSP00000408567.2:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12962C>G
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser47Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

3-183368289-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368289
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368289
    reference: chr 3
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.145G>A
  hgvsp: ENSP00000420207.1:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.145G>A
  hgvsp: ENSP00000416836.2:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.145G>A
  hgvsp: ENSP00000419010.1:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.145G>A
  hgvsp: ENSP00000419120.1:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.145G>A
  hgvsp: ENSP00000417347.1:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.145G>A
  hgvsp: ENSP00000417275.1:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12957G>A
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.145G>A
  hgvsp: ENSP00000242810.6:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.145G>A
  hgvsp: ENSP00000418922.1:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.145G>A
  hgvsp: ENSP00000408516.1:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.145G>A
  hgvsp: ENSP00000395012.1:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.145G>A
  hgvsp: ENSP00000408567.2:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala49Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

3-183368291-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368291
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368291
    reference: chr 3
allele count: 17
allele frequency: 1.400329489291598e-4
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.147C>T
  hgvsp: ENST00000454495.2:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.147C>T
  hgvsp: ENST00000476808.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.147C>T
  hgvsp: ENST00000242810.6:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.147C>T
  hgvsp: ENST00000473045.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.147C>T
  hgvsp: ENST00000454652.2:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12955C>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.147C>T
  hgvsp: ENST00000427201.2:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.147C>T
  hgvsp: ENST00000468001.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.147C>T
  hgvsp: ENST00000482138.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.147C>T
  hgvsp: ENST00000437402.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.147C>T
  hgvsp: ENST00000468101.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.147C>T
  hgvsp: ENST00000493074.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 19376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala49Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

3-183368292-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368292
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368292
    reference: chr 3
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.148G>A
  hgvsp: ENSP00000418922.1:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.148G>A
  hgvsp: ENSP00000419120.1:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.148G>A
  hgvsp: ENSP00000416836.2:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.148G>A
  hgvsp: ENSP00000395012.1:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.148G>A
  hgvsp: ENSP00000420207.1:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.148G>A
  hgvsp: ENSP00000242810.6:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.148G>A
  hgvsp: ENSP00000417347.1:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.148G>A
  hgvsp: ENSP00000408567.2:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.148G>A
  hgvsp: ENSP00000417275.1:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.148G>A
  hgvsp: ENSP00000419010.1:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.148G>A
  hgvsp: ENSP00000408516.1:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12954G>A
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Glu50Lys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/3-183368298-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368298
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368298
    reference: chr 3
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.154A>C
  hgvsp: ENSP00000417347.1:p.Ile52Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.154A>C
  hgvsp: ENSP00000418922.1:p.Ile52Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.154A>C
  hgvsp: ENSP00000408567.2:p.Ile52Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.154A>C
  hgvsp: ENSP00000419010.1:p.Ile52Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.154A>C
  hgvsp: ENSP00000395012.1:p.Ile52Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.154A>C
  hgvsp: ENSP00000242810.6:p.Ile52Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.154A>C
  hgvsp: ENSP00000420207.1:p.Ile52Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.154A>C
  hgvsp: ENSP00000419120.1:p.Ile52Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.154A>C
  hgvsp: ENSP00000408516.1:p.Ile52Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.154A>C
  hgvsp: ENSP00000417275.1:p.Ile52Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.154A>C
  hgvsp: ENSP00000416836.2:p.Ile52Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12948A>C
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile52Leu
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: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

3-183368316-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368316
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368316
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.172G>T
  hgvsp: ENSP00000419120.1:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.172G>T
  hgvsp: ENSP00000419010.1:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.172G>T
  hgvsp: ENSP00000420207.1:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12930G>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.172G>T
  hgvsp: ENSP00000417275.1:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.172G>T
  hgvsp: ENSP00000408516.1:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.172G>T
  hgvsp: ENSP00000395012.1:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.172G>T
  hgvsp: ENSP00000242810.6:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.172G>T
  hgvsp: ENSP00000417347.1:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.172G>T
  hgvsp: ENSP00000418922.1:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.172G>T
  hgvsp: ENSP00000408567.2:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.172G>T
  hgvsp: ENSP00000416836.2:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu58Ter
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

3-183368321-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368321
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368321
    reference: chr 3
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.177T>C
  hgvsp: ENST00000242810.6:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.177T>C
  hgvsp: ENST00000493074.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12925T>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.177T>C
  hgvsp: ENST00000454495.2:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.177T>C
  hgvsp: ENST00000437402.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.177T>C
  hgvsp: ENST00000476808.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.177T>C
  hgvsp: ENST00000482138.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.177T>C
  hgvsp: ENST00000427201.2:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.177T>C
  hgvsp: ENST00000468101.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.177T>C
  hgvsp: ENST00000468001.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.177T>C
  hgvsp: ENST00000454652.2:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.177T>C
  hgvsp: ENST00000473045.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe59Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

3-183368322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368322
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368322
    reference: chr 3
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.178C>T
  hgvsp: ENSP00000395012.1:p.Arg60Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.178C>T
  hgvsp: ENSP00000417347.1:p.Arg60Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.178C>T
  hgvsp: ENSP00000419010.1:p.Arg60Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.178C>T
  hgvsp: ENSP00000420207.1:p.Arg60Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.178C>T
  hgvsp: ENSP00000419120.1:p.Arg60Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408516
  ensembl transcript: ENST00000437402
  gene symbol: KLHL24
  hgvsc: ENST00000437402.1:c.178C>T
  hgvsp: ENSP00000408516.1:p.Arg60Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.178C>T
  hgvsp: ENSP00000242810.6:p.Arg60Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.178C>T
  hgvsp: ENSP00000408567.2:p.Arg60Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12924C>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.178C>T
  hgvsp: ENSP00000417275.1:p.Arg60Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.178C>T
  hgvsp: ENSP00000416836.2:p.Arg60Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.178C>T
  hgvsp: ENSP00000418922.1:p.Arg60Cys
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg60Cys
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

3-183368331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368331
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368331
    reference: chr 3
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.187C>T
  hgvsp: ENSP00000418922.1:p.Arg63Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.187C>T
  hgvsp: ENSP00000420207.1:p.Arg63Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.187C>T
  hgvsp: ENSP00000395012.1:p.Arg63Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.187C>T
  hgvsp: ENSP00000419120.1:p.Arg63Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.187C>T
  hgvsp: ENSP00000417347.1:p.Arg63Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.187C>T
  hgvsp: ENSP00000242810.6:p.Arg63Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.187C>T
  hgvsp: ENSP00000408567.2:p.Arg63Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.187C>T
  hgvsp: ENSP00000417275.1:p.Arg63Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.187C>T
  hgvsp: ENSP00000419010.1:p.Arg63Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12915C>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.187C>T
  hgvsp: ENSP00000416836.2:p.Arg63Cys
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg63Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

3-183368332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368332
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368332
    reference: chr 3
allele count: 11
allele frequency: 9.060358460727464e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.188G>A
  hgvsp: ENSP00000417347.1:p.Arg63His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.188G>A
  hgvsp: ENSP00000417275.1:p.Arg63His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.188G>A
  hgvsp: ENSP00000418922.1:p.Arg63His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.188G>A
  hgvsp: ENSP00000420207.1:p.Arg63His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.188G>A
  hgvsp: ENSP00000408567.2:p.Arg63His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.188G>A
  hgvsp: ENSP00000419120.1:p.Arg63His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.188G>A
  hgvsp: ENSP00000395012.1:p.Arg63His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12914G>A
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.188G>A
  hgvsp: ENSP00000419010.1:p.Arg63His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.188G>A
  hgvsp: ENSP00000242810.6:p.Arg63His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.188G>A
  hgvsp: ENSP00000416836.2:p.Arg63His
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg63His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

3-183368348-TATC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368348
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368345
    reference: chr 3
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12895_152-12893delCAT
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.207_209delCAT
  hgvsp: ENSP00000418922.1:p.Ile70del
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.207_209delCAT
  hgvsp: ENSP00000417275.1:p.Ile70del
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.207_209delCAT
  hgvsp: ENSP00000408567.2:p.Ile70del
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.207_209delCAT
  hgvsp: ENSP00000416836.2:p.Ile70del
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.207_209delCAT
  hgvsp: ENSP00000417347.1:p.Ile70del
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.207_209delCAT
  hgvsp: ENSP00000419120.1:p.Ile70del
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.207_209delCAT
  hgvsp: ENSP00000395012.1:p.Ile70del
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.207_209delCAT
  hgvsp: ENSP00000420207.1:p.Ile70del
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.207_209delCAT
  hgvsp: ENSP00000419010.1:p.Ile70del
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.207_209delCAT
  hgvsp: ENSP00000242810.6:p.Ile70del
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile70del
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: TATC
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

3-183368354-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368354
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368354
    reference: chr 3
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.210T>G
  hgvsp: ENSP00000417275.1:p.Ile70Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.210T>G
  hgvsp: ENSP00000416836.2:p.Ile70Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.210T>G
  hgvsp: ENSP00000417347.1:p.Ile70Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.210T>G
  hgvsp: ENSP00000419010.1:p.Ile70Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.210T>G
  hgvsp: ENSP00000420207.1:p.Ile70Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.210T>G
  hgvsp: ENSP00000242810.6:p.Ile70Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.210T>G
  hgvsp: ENSP00000418922.1:p.Ile70Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.210T>G
  hgvsp: ENSP00000408567.2:p.Ile70Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.210T>G
  hgvsp: ENSP00000395012.1:p.Ile70Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419120
  ensembl transcript: ENST00000473045
  gene symbol: KLHL24
  hgvsc: ENST00000473045.1:c.210T>G
  hgvsp: ENSP00000419120.1:p.Ile70Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12892T>G
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile70Met
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

3-183368364-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368364
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368364
    reference: chr 3
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.220G>C
  hgvsp: ENSP00000395012.1:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000420207
  ensembl transcript: ENST00000468101
  gene symbol: KLHL24
  hgvsc: ENST00000468101.1:c.220G>C
  hgvsp: ENSP00000420207.1:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.220G>C
  hgvsp: ENSP00000418922.1:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.220G>C
  hgvsp: ENSP00000419010.1:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.220G>C
  hgvsp: ENSP00000416836.2:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.220G>C
  hgvsp: ENSP00000417275.1:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12882G>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.220G>C
  hgvsp: ENSP00000417347.1:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.220G>C
  hgvsp: ENSP00000242810.6:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.220G>C
  hgvsp: ENSP00000408567.2:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly74Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

3-183368451-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368451
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368451
    reference: chr 3
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.307C>T
  hgvsp: ENSP00000419010.1:p.Arg103Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.307C>T
  hgvsp: ENSP00000416836.2:p.Arg103Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.307C>T
  hgvsp: ENSP00000242810.6:p.Arg103Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.307C>T
  hgvsp: ENSP00000408567.2:p.Arg103Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12795C>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.307C>T
  hgvsp: ENSP00000417275.1:p.Arg103Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.307C>T
  hgvsp: ENSP00000395012.1:p.Arg103Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.307C>T
  hgvsp: ENSP00000417347.1:p.Arg103Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.307C>T
  hgvsp: ENSP00000418922.1:p.Arg103Ter
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg103Ter
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

3-183368452-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368452
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368452
    reference: chr 3
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.308G>A
  hgvsp: ENSP00000408567.2:p.Arg103Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12794G>A
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.308G>A
  hgvsp: ENSP00000242810.6:p.Arg103Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.308G>A
  hgvsp: ENSP00000418922.1:p.Arg103Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.308G>A
  hgvsp: ENSP00000419010.1:p.Arg103Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.308G>A
  hgvsp: ENSP00000417347.1:p.Arg103Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.308G>A
  hgvsp: ENSP00000416836.2:p.Arg103Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.308G>A
  hgvsp: ENSP00000417275.1:p.Arg103Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.308G>A
  hgvsp: ENSP00000395012.1:p.Arg103Gln
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28257
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20134
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg103Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

3-183368458-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368458
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368458
    reference: chr 3
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.314T>C
  hgvsp: ENSP00000408567.2:p.Met105Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.314T>C
  hgvsp: ENSP00000419010.1:p.Met105Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.314T>C
  hgvsp: ENSP00000395012.1:p.Met105Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.314T>C
  hgvsp: ENSP00000417347.1:p.Met105Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.314T>C
  hgvsp: ENSP00000417275.1:p.Met105Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.314T>C
  hgvsp: ENSP00000418922.1:p.Met105Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.314T>C
  hgvsp: ENSP00000242810.6:p.Met105Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.314T>C
  hgvsp: ENSP00000416836.2:p.Met105Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12788T>C
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4407
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met105Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

3-183368483-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368483
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368483
    reference: chr 3
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.339A>G
  hgvsp: ENST00000482138.1:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12763A>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.339A>G
  hgvsp: ENST00000493074.1:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.339A>G
  hgvsp: ENST00000476808.1:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.339A>G
  hgvsp: ENST00000454495.2:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.339A>G
  hgvsp: ENST00000454652.2:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.339A>G
  hgvsp: ENST00000468001.1:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.339A>G
  hgvsp: ENST00000242810.6:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.339A>G
  hgvsp: ENST00000427201.2:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1800
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu113Leu
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP

3-183368485-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368485
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368485
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.341C>T
  hgvsp: ENSP00000417275.1:p.Ala114Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.341C>T
  hgvsp: ENSP00000395012.1:p.Ala114Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.341C>T
  hgvsp: ENSP00000418922.1:p.Ala114Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.341C>T
  hgvsp: ENSP00000416836.2:p.Ala114Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.341C>T
  hgvsp: ENSP00000417347.1:p.Ala114Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.341C>T
  hgvsp: ENSP00000242810.6:p.Ala114Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000408567
  ensembl transcript: ENST00000427201
  gene symbol: KLHL24
  hgvsc: ENST00000427201.2:c.341C>T
  hgvsp: ENST00000427201.2:c.341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.341C>T
  hgvsp: ENSP00000419010.1:p.Ala114Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12761C>T
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala114Val
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

3-183368489-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368489
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368489
    reference: chr 3
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.345A>T
  hgvsp: ENSP00000417275.1:p.Glu115Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12757A>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417347
  ensembl transcript: ENST00000493074
  gene symbol: KLHL24
  hgvsc: ENST00000493074.1:c.345A>T
  hgvsp: ENSP00000417347.1:p.Glu115Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000418922
  ensembl transcript: ENST00000468001
  gene symbol: KLHL24
  hgvsc: ENST00000468001.1:c.345A>T
  hgvsp: ENSP00000418922.1:p.Glu115Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.345A>T
  hgvsp: ENSP00000395012.1:p.Glu115Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.345A>T
  hgvsp: ENSP00000419010.1:p.Glu115Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000416836
  ensembl transcript: ENST00000454495
  gene symbol: KLHL24
  hgvsc: ENST00000454495.2:c.345A>T
  hgvsp: ENSP00000416836.2:p.Glu115Asp
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.345A>T
  hgvsp: ENSP00000242810.6:p.Glu115Asp
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4407
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu115Asp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP

3-183368527-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368527
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368527
    reference: chr 3
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12719A>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.383A>G
  hgvsp: ENSP00000419010.1:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.383A>G
  hgvsp: ENSP00000242810.6:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000417275
  ensembl transcript: ENST00000482138
  gene symbol: KLHL24
  hgvsc: ENST00000482138.1:c.383A>G
  hgvsp: ENSP00000417275.1:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.383A>G
  hgvsp: ENSP00000395012.1:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28271
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4407
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20133
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys128Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-183368553-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368553
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368553
    reference: chr 3
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12693C>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.409C>T
  hgvsp: ENSP00000395012.1:p.Gln137Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.409C>T
  hgvsp: ENSP00000242810.6:p.Gln137Ter
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.409C>T
  hgvsp: ENSP00000419010.1:p.Gln137Ter
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28263
  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: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1800
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4401
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20132
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln137Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

3-183368582-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368582
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368582
    reference: chr 3
allele count: 6
allele frequency: 4.943886883868097e-5
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12664T>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.438T>G
  hgvsp: ENSP00000395012.1:p.Phe146Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.438T>G
  hgvsp: ENSP00000242810.6:p.Phe146Leu
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.438T>G
  hgvsp: ENSP00000419010.1:p.Phe146Leu
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1854
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 1400
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genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4389
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20135
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe146Leu
num of homozygotes: 1
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

3-183368586-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368586
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368586
    reference: chr 3
allele count: 29
allele frequency: 2.389742237457973e-4
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.442A>G
  hgvsp: ENSP00000395012.1:p.Ile148Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.442A>G
  hgvsp: ENSP00000242810.6:p.Ile148Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12660A>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.442A>G
  hgvsp: ENSP00000419010.1:p.Ile148Val
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11583
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1398
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1850
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 1053
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genotype quality: GenotypeQuality
  all individuals: 8
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4380
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ile148Val
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

3-183368588-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368588
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368588
    reference: chr 3
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.444T>G
  hgvsp: ENSP00000419010.1:p.Ile148Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12658T>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.444T>G
  hgvsp: ENSP00000395012.1:p.Ile148Met
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.444T>G
  hgvsp: ENSP00000242810.6:p.Ile148Met
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1851
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20131
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile148Met
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

3-183368599-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368599
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368599
    reference: chr 3
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.455G>A
  hgvsp: ENSP00000419010.1:p.Arg152His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.455G>A
  hgvsp: ENSP00000242810.6:p.Arg152His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.455G>A
  hgvsp: ENSP00000395012.1:p.Arg152His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12647G>A
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20131
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28005
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4359
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg152His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

3-183368606-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368606
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368606
    reference: chr 3
allele count: 2
allele frequency: 1.648804616652927e-5
allele num: 121300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.462A>G
  hgvsp: ENST00000242810.6:c.462A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.462A>G
  hgvsp: ENST00000476808.1:c.462A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12640A>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.462A>G
  hgvsp: ENST00000454652.2:c.462A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1052
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20130
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 28029
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1844
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala154Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

3-183368607-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368607
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368607
    reference: chr 3
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.463T>C
  hgvsp: ENSP00000242810.6:p.Cys155Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.463T>C
  hgvsp: ENSP00000395012.1:p.Cys155Arg
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12639T>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.463T>C
  hgvsp: ENSP00000419010.1:p.Cys155Arg
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1052
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28010
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20129
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4359
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1844
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1747
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Cys155Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

3-183368630-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368630
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368630
    reference: chr 3
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.486A>G
  hgvsp: ENST00000242810.6:c.486A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12616A>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.486A>G
  hgvsp: ENST00000454652.2:c.486A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.486A>G
  hgvsp: ENST00000476808.1:c.486A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27945
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4327
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20131
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1836
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln162Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

3-183368639-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368639
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368639
    reference: chr 3
allele count: 4
allele frequency: 3.29918675046601e-5
allele num: 121242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.495T>C
  hgvsp: ENST00000476808.1:c.495T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.495T>C
  hgvsp: ENST00000454652.2:c.495T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.495T>C
  hgvsp: ENST00000242810.6:c.495T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12607T>C
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 20127
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1830
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4326
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro165Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

3-183368641-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368641
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368641
    reference: chr 3
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.497G>C
  hgvsp: ENSP00000242810.6:p.Cys166Ser
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.497G>C
  hgvsp: ENSP00000395012.1:p.Cys166Ser
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.497G>C
  hgvsp: ENSP00000419010.1:p.Cys166Ser
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12605G>C
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4326
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27879
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20125
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys166Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

3-183368642-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368642
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368642
    reference: chr 3
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.498T>C
  hgvsp: ENST00000242810.6:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.498T>C
  hgvsp: ENST00000476808.1:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12604T>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.498T>C
  hgvsp: ENST00000454652.2:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4323
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27867
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys166Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

3-183368646-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368646
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368646
    reference: chr 3
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.502T>A
  hgvsp: ENSP00000419010.1:p.Cys168Ser
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12600T>A
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.502T>A
  hgvsp: ENSP00000242810.6:p.Cys168Ser
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.502T>A
  hgvsp: ENSP00000395012.1:p.Cys168Ser
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20124
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27835
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Cys168Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-183368662-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368662
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368662
    reference: chr 3
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.518G>A
  hgvsp: ENSP00000395012.1:p.Arg173His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12584G>A
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.518G>A
  hgvsp: ENSP00000419010.1:p.Arg173His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.518G>A
  hgvsp: ENSP00000242810.6:p.Arg173His
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27762
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20122
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1830
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg173His
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

3-183368663-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368663
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368663
    reference: chr 3
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.519C>G
  hgvsp: ENST00000242810.6:c.519C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12583C>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.519C>G
  hgvsp: ENST00000454652.2:c.519C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.519C>G
  hgvsp: ENST00000476808.1:c.519C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4311
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg173Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

3-183368663-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368663
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368663
    reference: chr 3
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.519C>T
  hgvsp: ENST00000454652.2:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.519C>T
  hgvsp: ENST00000476808.1:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12583C>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.519C>T
  hgvsp: ENST00000242810.6:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4311
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27745
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg173Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

3-183368672-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368672
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368672
    reference: chr 3
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.528T>C
  hgvsp: ENST00000454652.2:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.528T>C
  hgvsp: ENST00000242810.6:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.528T>C
  hgvsp: ENST00000476808.1:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12574T>C
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1827
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27710
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20124
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp176Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

3-183368674-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368674
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368674
    reference: chr 3
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.530C>T
  hgvsp: ENSP00000419010.1:p.Thr177Ile
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.530C>T
  hgvsp: ENSP00000395012.1:p.Thr177Ile
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.530C>T
  hgvsp: ENSP00000242810.6:p.Thr177Ile
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12572C>T
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4315
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20124
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27657
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr177Ile
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

3-183368678-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368678
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368678
    reference: chr 3
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.534T>A
  hgvsp: ENSP00000395012.1:p.His178Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.534T>A
  hgvsp: ENSP00000242810.6:p.His178Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12568T>A
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.534T>A
  hgvsp: ENSP00000419010.1:p.His178Gln
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4316
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1828
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1747
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His178Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

3-183368689-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368689
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368689
    reference: chr 3
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.545C>T
  hgvsp: ENSP00000419010.1:p.Thr182Ile
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.545C>T
  hgvsp: ENSP00000242810.6:p.Thr182Ile
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12557C>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.545C>T
  hgvsp: ENSP00000395012.1:p.Thr182Ile
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 51
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1747
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
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genotype quality: GenotypeQuality
  all individuals: 1826
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 9
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1797
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20122
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4311
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr182Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

3-183368690-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368690
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368690
    reference: chr 3
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.546A>G
  hgvsp: ENST00000476808.1:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12556A>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.546A>G
  hgvsp: ENST00000242810.6:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.546A>G
  hgvsp: ENST00000454652.2:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20123
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4316
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27689
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr182Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

3-183368696-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368696
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368696
    reference: chr 3
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.552C>T
  hgvsp: ENST00000242810.6:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.552C>T
  hgvsp: ENST00000454652.2:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.552C>T
  hgvsp: ENST00000476808.1:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12550C>T
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27701
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1828
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Phe184Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/3-183368697-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368697
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368697
    reference: chr 3
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.553A>C
  hgvsp: ENSP00000395012.1:p.Thr185Pro
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.553A>C
  hgvsp: ENSP00000419010.1:p.Thr185Pro
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.553A>C
  hgvsp: ENSP00000242810.6:p.Thr185Pro
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12549A>C
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1827
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4321
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20124
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27726
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr185Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

3-183368702-ATG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368702
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368700
    reference: chr 3
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12543_152-12542delTG
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.559_560delTG
  hgvsp: ENSP00000242810.6:p.Cys187GlnfsTer9
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.559_560delTG
  hgvsp: ENSP00000419010.1:p.Cys187GlnfsTer9
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.559_560delTG
  hgvsp: ENSP00000395012.1:p.Cys187GlnfsTer9
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27801
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20124
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1747
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 4326
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1829
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Cys187GlnfsTer9
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: ATG
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

3-183368723-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368723
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368723
    reference: chr 3
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.579G>A
  hgvsp: ENST00000476808.1:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.579G>A
  hgvsp: ENST00000454652.2:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.579G>A
  hgvsp: ENST00000242810.6:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12523G>A
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4338
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20125
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27916
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln193Gln
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum

3-183368723-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368723
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368723
    reference: chr 3
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.579G>C
  hgvsp: ENSP00000242810.6:p.Gln193His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.579G>C
  hgvsp: ENSP00000419010.1:p.Gln193His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.579G>C
  hgvsp: ENSP00000395012.1:p.Gln193His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12523G>C
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1750
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4338
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1830
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27916
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln193His
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-183368726-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368726
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368726
    reference: chr 3
allele count: 53
allele frequency: 4.372215805972612e-4
allele num: 121220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.582T>A
  hgvsp: ENST00000242810.6:c.582T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12520T>A
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.582T>A
  hgvsp: ENST00000454652.2:c.582T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.582T>A
  hgvsp: ENST00000476808.1:c.582T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 9.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20162
  bin: 9.75e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27941
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr194Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

3-183368728-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368728
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368728
    reference: chr 3
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.584T>G
  hgvsp: ENSP00000242810.6:p.Phe195Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12518T>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.584T>G
  hgvsp: ENSP00000419010.1:p.Phe195Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.584T>G
  hgvsp: ENSP00000395012.1:p.Phe195Cys
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20122
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27955
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4338
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1832
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe195Cys
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/3-183368734-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368734
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368734
    reference: chr 3
allele count: 235
allele frequency: 1.938144329896907e-3
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12512A>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.590A>C
  hgvsp: ENSP00000395012.1:p.Asp197Ala
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.590A>C
  hgvsp: ENSP00000419010.1:p.Asp197Ala
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.590A>C
  hgvsp: ENSP00000242810.6:p.Asp197Ala
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 9.75e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27940
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1384
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1791
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp197Ala
num of homozygotes: 2
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-183368734-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368734
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368734
    reference: chr 3
allele count: 3
allele frequency: 2.474226804123711e-5
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.590A>T
  hgvsp: ENSP00000242810.6:p.Asp197Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.590A>T
  hgvsp: ENSP00000419010.1:p.Asp197Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.590A>T
  hgvsp: ENSP00000395012.1:p.Asp197Val
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12512A>T
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20273
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp197Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

3-183368736-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368736
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368736
    reference: chr 3
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.592G>A
  hgvsp: ENSP00000242810.6:p.Val198Ile
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12510G>A
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.592G>A
  hgvsp: ENSP00000419010.1:p.Val198Ile
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.592G>A
  hgvsp: ENSP00000395012.1:p.Val198Ile
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1750
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4339
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20097
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
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genotype quality: GenotypeQuality
  all individuals: 28048
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1827
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val198Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

3-183368747-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368747
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368747
    reference: chr 3
allele count: 1951
allele frequency: 1.60835586625338e-2
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12499C>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.603C>T
  hgvsp: ENST00000454652.2:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.603C>T
  hgvsp: ENST00000476808.1:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.603C>T
  hgvsp: ENST00000242810.6:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 8.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 6.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 9.75e1
  variant carriers: 1111
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 6.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 18848
  bin: 2.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 11358
  bin: 2.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 95
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4236
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20955
  bin: 9.75e1
  variant carriers: 1776
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1776
  bin: 9.25e1
  variant carriers: 0
hgvs: p.His201His
num of homozygotes: 163
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-183368766-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368766
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368766
    reference: chr 3
allele count: 8
allele frequency: 6.593805120089676e-5
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12480G>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.622G>C
  hgvsp: ENSP00000242810.6:p.Asp208His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.622G>C
  hgvsp: ENSP00000395012.1:p.Asp208His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.622G>C
  hgvsp: ENSP00000419010.1:p.Asp208His
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19848
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1821
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1758
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4410
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28334
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp208His
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

3-183368798-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368798
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368798
    reference: chr 3
allele count: 4
allele frequency: 3.295978905735003e-5
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.654T>C
  hgvsp: ENST00000242810.6:c.654T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12448T>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.654T>C
  hgvsp: ENST00000454652.2:c.654T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.654T>C
  hgvsp: ENST00000476808.1:c.654T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1824
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1823
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19843
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser218Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

3-183368812-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368812
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368812
    reference: chr 3
allele count: 4
allele frequency: 3.295653033648617e-5
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12434T>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.668T>C
  hgvsp: ENSP00000242810.6:p.Ile223Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.668T>C
  hgvsp: ENSP00000395012.1:p.Ile223Thr
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.668T>C
  hgvsp: ENSP00000419010.1:p.Ile223Thr
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4438
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28444
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19842
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1824
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile223Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

3-183368825-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368825
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368825
    reference: chr 3
allele count: 4
allele frequency: 3.295164346321773e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.681G>A
  hgvsp: ENST00000242810.6:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.681G>A
  hgvsp: ENST00000454652.2:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12421G>A
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.681G>A
  hgvsp: ENST00000476808.1:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 8.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19842
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
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genotype quality: GenotypeQuality
  all individuals: 14
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28435
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu227Glu
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

3-183368835-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368835
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368835
    reference: chr 3
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12411G>C
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.691G>C
  hgvsp: ENSP00000242810.6:p.Glu231Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.691G>C
  hgvsp: ENSP00000395012.1:p.Glu231Gln
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.691G>C
  hgvsp: ENSP00000419010.1:p.Glu231Gln
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4439
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1828
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu231Gln
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

3-183368840-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368840
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368840
    reference: chr 3
allele count: 5
allele frequency: 4.119294776734223e-5
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.696C>T
  hgvsp: ENST00000476808.1:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12406C>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.696C>T
  hgvsp: ENST00000242810.6:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.696C>T
  hgvsp: ENST00000454652.2:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11883
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1830
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19846
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28390
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala232Ala
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

3-183368841-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368841
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368841
    reference: chr 3
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.697G>A
  hgvsp: ENSP00000395012.1:p.Val233Ile
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.697G>A
  hgvsp: ENSP00000419010.1:p.Val233Ile
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.697G>A
  hgvsp: ENSP00000242810.6:p.Val233Ile
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12405G>A
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4422
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1830
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28386
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19842
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val233Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

3-183368847-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368847
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368847
    reference: chr 3
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.703C>T
  hgvsp: ENSP00000419010.1:p.Arg235Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12399C>T
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.703C>T
  hgvsp: ENSP00000395012.1:p.Arg235Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.703C>T
  hgvsp: ENSP00000242810.6:p.Arg235Cys
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4050
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1828
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28386
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1823
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg235Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

3-183368848-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368848
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368848
    reference: chr 3
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12398G>A
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.704G>A
  hgvsp: ENSP00000242810.6:p.Arg235His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.704G>A
  hgvsp: ENSP00000419010.1:p.Arg235His
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.704G>A
  hgvsp: ENSP00000395012.1:p.Arg235His
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4416
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28400
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19836
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1825
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg235His
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS

3-183368857-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 183368857
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 183368857
    reference: chr 3
allele count: 3
allele frequency: 2.471902705909495e-5
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000395012
  ensembl transcript: ENST00000454652
  gene symbol: KLHL24
  hgvsc: ENST00000454652.2:c.713A>G
  hgvsp: ENSP00000395012.1:p.Tyr238Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114796
  ensembl transcript: ENST00000475827
  gene symbol: KLHL24
  hgvsc: ENST00000475827.1:n.152-12389A>G
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000419010
  ensembl transcript: ENST00000476808
  gene symbol: KLHL24
  hgvsc: ENST00000476808.1:c.713A>G
  hgvsp: ENSP00000419010.1:p.Tyr238Cys
  variant of: http://identifiers.org/hgnc/25947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114796
  ensembl protein: ENSP00000242810
  ensembl transcript: ENST00000242810
  gene symbol: KLHL24
  hgvsc: ENST00000242810.6:c.713A>G
  hgvsp: ENSP00000242810.6:p.Tyr238Cys
  variant of: http://identifiers.org/hgnc/25947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Tyr238Cys
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 5578
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 144
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7113
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2020
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40456
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 837
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 349
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3301
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2342
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.026694045174538e-4
allele num: 9740
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
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: 6612
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.006253006253006e-5
allele num: 66528
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.13e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

FS
type: SiteQuality
SIO_000300: 8.802e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

DP
type: SiteQuality
SIO_000300: 1.554969e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

GenotypeDepth
all individuals: 101
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1570
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 245
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2347
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2028
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7136
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2974
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3348
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40611
bin: 6.25e1
variant carriers: 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: 1.499655079331754e-5
allele num: 66682
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: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.204e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 3.151e0

QD
type: SiteQuality
SIO_000300: 1.561e1

DP
type: SiteQuality
SIO_000300: 1.560138e6

GenotypeDepth
all individuals: 2765
bin: 7.25e1
variant carriers: 2750

GenotypeDepth
all individuals: 2733
bin: 6.75e1
variant carriers: 2707

GenotypeDepth
all individuals: 2281
bin: 8.25e1
variant carriers: 2278

GenotypeDepth
all individuals: 1876
bin: 8.75e1
variant carriers: 1872

GenotypeQuality
all individuals: 634
bin: 7.25e1
variant carriers: 18

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 12

GenotypeQuality
all individuals: 29300
bin: 9.75e1
variant carriers: 28902

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 14

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 17

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 9

GenotypeQuality
all individuals: 280
bin: 8.25e1
variant carriers: 27

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 14

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 88
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 3219
bin: 6.75e1
variant carriers: 16

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 2

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

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 8

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 23

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 10

GenotypeQuality
all individuals: 26094
bin: 6.25e1
variant carriers: 16

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 140
bin: 9.25e1
variant carriers: 36

GenotypeQuality
all individuals: 617
bin: 7.75e1
variant carriers: 15

Latino
type: Population
allele count: 3332
allele frequency: 2.881854350458398e-1
allele num: 11562
num of homozygotes: 476

South Asian
type: Population
allele count: 3130
allele frequency: 1.895591085271318e-1
allele num: 16512
num of homozygotes: 333

African
type: Population
allele count: 5043
allele frequency: 4.974353915959756e-1
allele num: 10138
num of homozygotes: 1245

European (Finnish)
type: Population
allele count: 1427
allele frequency: 2.157544602358633e-1
allele num: 6614
num of homozygotes: 156

European (Non-Finnish)
type: Population
allele count: 17358
allele frequency: 2.602632920502594e-1
allele num: 66694
num of homozygotes: 2283

Other
type: Population
allele count: 265
allele frequency: 2.918502202643172e-1
allele num: 908
num of homozygotes: 36

East Asian
type: Population
allele count: 4041
allele frequency: 4.671676300578035e-1
allele num: 8650
num of homozygotes: 965

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.3e0

DP
type: SiteQuality
SIO_000300: 3.098133e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.322e0

QD
type: SiteQuality
SIO_000300: 1.734e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.11e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 1579
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11596
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5050
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 473
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28005
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 95
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1800
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1058
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1760
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20154
bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.436e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.95e0

MQRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

VQSLOD
type: SiteQuality
SIO_000300: -1.295e0

QD
type: SiteQuality
SIO_000300: 1.946e1

DP
type: SiteQuality
SIO_000300: 2.283838e6

GenotypeDepth
all individuals: 830
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4123
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 473
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5047
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28071
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4416
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1760
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1871
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1411
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20153
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1059
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 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: 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: 10290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.005e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.469e0

DP
type: SiteQuality
SIO_000300: 2.284751e6

MQ
type: SiteQuality
SIO_000300: 5.981e1

MQRankSum
type: SiteQuality
SIO_000300: -4.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 9.419999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.33e-1

GenotypeDepth
all individuals: 3923
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3141
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1579
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 473
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28094
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1760
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4415
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1800
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20151
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1413
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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African
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East Asian
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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DP
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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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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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East Asian
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ReadPosRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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ClippingRankSum
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MQ
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DP
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QD
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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FS
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DP
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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South Asian
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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QD
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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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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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DP
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QD
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European (Finnish)
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African
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeQuality
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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DP
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MQ
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FS
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VQSLOD
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GenotypeQuality
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African
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DP
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MQ
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African
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MQ
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VQSLOD
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East Asian
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DP
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VQSLOD
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VQSLOD
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ReadPosRankSum
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SIO_000300: 4.28e-1

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

GenotypeQuality
all individuals: 1799
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28249
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1861
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1754
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 20141
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4405
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1406
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.37e-1

DP
type: SiteQuality
SIO_000300: 2.285936e6

MQ
type: SiteQuality
SIO_000300: 5.987e1

FS
type: SiteQuality
SIO_000300: 3.274e0

MQRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-1

QD
type: SiteQuality
SIO_000300: 1.125e1

GenotypeDepth
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 9.75e1
variant carriers: 11

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.039981511439797e-3
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
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 (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

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.09e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.88e-1

FS
type: SiteQuality
SIO_000300: 1.104e0

DP
type: SiteQuality
SIO_000300: 2.286623e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.189e1

GenotypeDepth
all individuals: 19413
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 28268
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variant carriers: 0

GenotypeQuality
all individuals: 1800
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

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

Latino
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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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.28574e6

VQSLOD
type: SiteQuality
SIO_000300: 3.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.693e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.701e0

MQRankSum
type: SiteQuality
SIO_000300: -1.494e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.48e-1

QD
type: SiteQuality
SIO_000300: 1.895e1

GenotypeDepth
all individuals: 281
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variant carriers: 0

GenotypeQuality
all individuals: 4408
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1756
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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: 0
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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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1860
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
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: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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: 11576
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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 2.285723e6

FS
type: SiteQuality
SIO_000300: 2.9578e1

QD
type: SiteQuality
SIO_000300: 7.9e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.53e0

VQSLOD
type: SiteQuality
SIO_000300: -4.671e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeQuality
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bin: 8.75e1
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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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: 1403
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1858
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.285781e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.504e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.0e-2

FS
type: SiteQuality
SIO_000300: 2.179e0

QD
type: SiteQuality
SIO_000300: 1.396e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.56e-2

MQ
type: SiteQuality
SIO_000300: 5.984e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-1

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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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

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: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 2.285694e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.845e0

VQSLOD
type: SiteQuality
SIO_000300: -6.839e-1

FS
type: SiteQuality
SIO_000300: 3.317e0

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

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 1.49e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
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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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
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: 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

MQ
type: SiteQuality
SIO_000300: 5.987e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

MQRankSum
type: SiteQuality
SIO_000300: 6.61e-1

FS
type: SiteQuality
SIO_000300: 1.32e0

VQSLOD
type: SiteQuality
SIO_000300: 6.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.956e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.285667e6

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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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SIO_000300: 3.34e-1

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

MQ
type: SiteQuality
SIO_000300: 5.988e1

QD
type: SiteQuality
SIO_000300: 1.344e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.16e-1

DP
type: SiteQuality
SIO_000300: 2.285592e6

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

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

African
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.8e-1

ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.015e1

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

Latino
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allele num: 11578
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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MQ
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BaseQRankSum
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SIO_000300: -7.216e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.91e-1

DP
type: SiteQuality
SIO_000300: 2.285553e6

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

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

Other
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.987e1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

African
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num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.288e0

DP
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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ReadPosRankSum
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MQ
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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East Asian
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num of homozygotes: 0

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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Latino
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South Asian
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allele num: 16510
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African
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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QD
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 29

GenotypeQuality
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variant carriers: 0

East Asian
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num of homozygotes: 0

Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
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European (Finnish)
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European (Non-Finnish)
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allele count: 24
allele frequency: 3.598740440845704e-4
allele num: 66690
num of homozygotes: 0

Other
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South Asian
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allele frequency: 2.422774076317383e-4
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QD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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DP
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FS
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

East Asian
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allele num: 8652
num of homozygotes: 0

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 10378
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.281282e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

FS
type: SiteQuality
SIO_000300: 6.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.329e0

VQSLOD
type: SiteQuality
SIO_000300: 2.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.53e-1

QD
type: SiteQuality
SIO_000300: 1.475e1

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
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: 16504
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.131e0

QD
type: SiteQuality
SIO_000300: 1.342e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.23e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.982e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.279855e6

MQ
type: SiteQuality
SIO_000300: 5.986e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e0

MQRankSum
type: SiteQuality
SIO_000300: -2.688e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1746
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 7.25e1
variant carriers: 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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.00294144130624e-5
allele num: 66634
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.773e0

QD
type: SiteQuality
SIO_000300: 1.48e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.11e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.82e-1

DP
type: SiteQuality
SIO_000300: 2.279039e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 16504
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 7.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

QD
type: SiteQuality
SIO_000300: 1.529e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.45e-1

DP
type: SiteQuality
SIO_000300: 2.278742e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.77e-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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GenotypeQuality
all individuals: 92
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.313e0

QD
type: SiteQuality
SIO_000300: 1.68e1

DP
type: SiteQuality
SIO_000300: 2.278676e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.79e0

VQSLOD
type: SiteQuality
SIO_000300: -9.603e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e0

FS
type: SiteQuality
SIO_000300: 6.599e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1050
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.403e1

FS
type: SiteQuality
SIO_000300: 7.024e0

DP
type: SiteQuality
SIO_000300: 2.278195e6

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

MQ
type: SiteQuality
SIO_000300: 5.915e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.19e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.165e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.53e-1

QD
type: SiteQuality
SIO_000300: 1.349e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

DP
type: SiteQuality
SIO_000300: 2.27714e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -6.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.6e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27745
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

DP
type: SiteQuality
SIO_000300: 2.277057e6

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

MQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.964e0

QD
type: SiteQuality
SIO_000300: 1.388e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
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: 1
allele frequency: 9.665571235260003e-5
allele num: 10346
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.964e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 5.75e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.277057e6

MQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

QD
type: SiteQuality
SIO_000300: 1.388e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.22e-1

FS
type: SiteQuality
SIO_000300: 5.559e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.401e1

MQ
type: SiteQuality
SIO_000300: 5.933e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.071e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1826
bin: 7.75e1
variant carriers: 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: 10340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.168e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.276496e6

QD
type: SiteQuality
SIO_000300: 1.29e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 120
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
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: 8648
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.24e-1

FS
type: SiteQuality
SIO_000300: 2.247e0

DP
type: SiteQuality
SIO_000300: 2.27637e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

MQ
type: SiteQuality
SIO_000300: 5.923e1

QD
type: SiteQuality
SIO_000300: 9.59e0

VQSLOD
type: SiteQuality
SIO_000300: -4.85e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.04e-1

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 9.689922480620155e-5
allele num: 10320
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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BaseQRankSum
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DP
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QD
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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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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variant carriers: 0

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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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
allele num: 16500
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European (Non-Finnish)
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allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

ReadPosRankSum
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MQ
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FS
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BaseQRankSum
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QD
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DP
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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VQSLOD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10316
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

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

VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 1.699e0

BaseQRankSum
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MQRankSum
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MQ
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ReadPosRankSum
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DP
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SIO_000300: 2.276615e6

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: 8648
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
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VQSLOD
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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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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variant carriers: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.982e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

FS
type: SiteQuality
SIO_000300: 2.849e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e0

DP
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SIO_000300: 2.27726e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.016e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 906
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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10306
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

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.4641e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 2.27854e6

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

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

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

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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DP
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ClippingRankSum
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SIO_000300: 6.1e-2

ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

Latino
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allele frequency: 4.494382022471911e-3
allele num: 11570
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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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 frequency: 0.0e0
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Other
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
type: SiteQuality
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FS
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ReadPosRankSum
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DP
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ClippingRankSum
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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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Latino
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African
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East Asian
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South Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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allele frequency: 1.499880009599232e-5
allele num: 66672
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InbreedingCoeff
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ReadPosRankSum
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QD
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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ClippingRankSum
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DP
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MQ
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GenotypeQuality
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variant carriers: 233

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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African
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South Asian
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East Asian
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European (Non-Finnish)
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allele frequency: 1.049664107485605e-4
allele num: 66688
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Latino
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MQ
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FS
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MQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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DP
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ReadPosRankSum
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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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East Asian
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European (Finnish)
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African
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South Asian
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Latino
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Other
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European (Non-Finnish)
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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FS
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DP
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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Latino
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Other
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European (Non-Finnish)
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African
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ReadPosRankSum
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DP
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1703
bin: 8.25e1
variant carriers: 3

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

Latino
type: Population
allele count: 82
allele frequency: 7.084845343010195e-3
allele num: 11574
num of homozygotes: 1

African
type: Population
allele count: 1814
allele frequency: 1.754352030947776e-1
allele num: 10340
num of homozygotes: 162

Other
type: Population
allele count: 5
allele frequency: 5.518763796909493e-3
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.029568589432865e-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

East Asian
type: Population
allele count: 7
allele frequency: 8.092485549132948e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 38
allele frequency: 5.695785119011931e-4
allele num: 66716
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.485e1

DP
type: SiteQuality
SIO_000300: 2.386466e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.493e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.59e0

FS
type: SiteQuality
SIO_000300: 5.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.198861081972126e-4
allele num: 66730
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: 10334
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: 5.935e1

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.97e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

QD
type: SiteQuality
SIO_000300: 1.256e1

DP
type: SiteQuality
SIO_000300: 2.269773e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.81e-1

GenotypeQuality
all individuals: 1432
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28427
bin: 6.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 10366
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: 16510
num of homozygotes: 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

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

FS
type: SiteQuality
SIO_000300: 2.635e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-1

DP
type: SiteQuality
SIO_000300: 2.27072e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.32e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: -7.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.51e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

GenotypeQuality
all individuals: 1824
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

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

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: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.99e0

FS
type: SiteQuality
SIO_000300: 1.0348e1

MQRankSum
type: SiteQuality
SIO_000300: 8.45e-1

QD
type: SiteQuality
SIO_000300: 1.51e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.999000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 2.270743e6

GenotypeQuality
all individuals: 4440
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1826
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.622140050843541e-4
allele num: 8654
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: 16510
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

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

QD
type: SiteQuality
SIO_000300: 1.06e1

MQ
type: SiteQuality
SIO_000300: 5.978e1

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.26e-1

FS
type: SiteQuality
SIO_000300: 2.984e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.724e0

DP
type: SiteQuality
SIO_000300: 2.270907e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.55e-1

GenotypeQuality
all individuals: 19843
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 0
allele frequency: 0.0e0
allele num: 66732
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: 6612
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

DP
type: SiteQuality
SIO_000300: 2.270553e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.15e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.363e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.81e-1

QD
type: SiteQuality
SIO_000300: 1.533e1

VQSLOD
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1429
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4428
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1825
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495594317568783e-5
allele num: 66732
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.71e-1

DP
type: SiteQuality
SIO_000300: 2.27063e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.09e-1

FS
type: SiteQuality
SIO_000300: 4.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
all individuals: 1823
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1078
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.691e0

MQRankSum
type: SiteQuality
SIO_000300: -1.592e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.849e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 2.267e0

VQSLOD
type: SiteQuality
SIO_000300: -2.223e0

DP
type: SiteQuality
SIO_000300: 2.270493e6

QD
type: SiteQuality
SIO_000300: 9.359999999999999e0

GenotypeQuality
all individuals: 19839
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4416
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.37e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

FS
type: SiteQuality
SIO_000300: 1.498e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.345e0

QD
type: SiteQuality
SIO_000300: 2.51e0

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.270339e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.58e-1

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

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1828
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

QD
type: SiteQuality
SIO_000300: 1.23e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.13e-1

DP
type: SiteQuality
SIO_000300: 2.270239e6

FS
type: SiteQuality
SIO_000300: 1.127e0