http://identifiers.org/exac.variant/12-10462126-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462126
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462126
    reference: chr 12
allele count: 9
allele frequency: 7.589940798461771e-5
allele num: 118578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1800C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.100+47C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.100+47C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.100+47C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+47C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.100+47C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.100+47C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.141-99C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.8-99C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.8-99C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.100+47C>A
  variant of: http://identifiers.org/hgnc/6378
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12218
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9899
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9110
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11635
  bin: 9.75e1
  variant carriers: 9
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

12-10462192-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462192
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462192
    reference: chr 12
allele count: 1
allele frequency: 8.921561630147741e-6
allele num: 112088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.101-33C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.101-33C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.8-33C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.8-33C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1866C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.101-33C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.101-33C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+113C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.141-33C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.101-33C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.101-33C>T
  variant of: http://identifiers.org/hgnc/6378
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10401
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5967
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

12-10462208-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462208
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462208
    reference: chr 12
allele count: 1
allele frequency: 8.78966335589347e-6
allele num: 113770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+129C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.8-17C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.101-17C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1882C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.101-17C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.101-17C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.141-17C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.101-17C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.101-17C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.8-17C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.101-17C>G
  variant of: http://identifiers.org/hgnc/6378
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

12-10462210-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462210
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462210
    reference: chr 12
allele count: 1
allele frequency: 8.748600223964166e-6
allele num: 114304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.101-15A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.101-15A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.8-15A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+131A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.101-15A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.8-15A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.101-15A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1884A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.101-15A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.141-15A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.101-15A>G
  variant of: http://identifiers.org/hgnc/6378
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ

12-10462221-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462221
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462221
    reference: chr 12
allele count: 20
allele frequency: 1.719601740236961e-4
allele num: 116306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.101-4A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.8-4A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.101-4A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.141-4A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.8-4A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.101-4A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.101-4A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.101-4A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1895A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+142A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.101-4A>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29351
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13259
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: c.101-4A>G
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

12-10462227-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462227
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462227
    reference: chr 12
allele count: 1
allele frequency: 8.527911855503062e-6
allele num: 117262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.103T>C
  hgvsp: ENSP00000344858.6:p.Phe35Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.103T>C
  hgvsp: ENSP00000438514.1:p.Phe35Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.103T>C
  hgvsp: ENSP00000338130.4:p.Phe35Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.10T>C
  hgvsp: ENSP00000310929.7:p.Phe4Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.103T>C
  hgvsp: ENSP00000441074.1:p.Phe35Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+148T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1901T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.103T>C
  hgvsp: ENSP00000371333.3:p.Phe35Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.10T>C
  hgvsp: ENSP00000438669.1:p.Phe4Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.143T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.103T>C
  hgvsp: ENSP00000371332.4:p.Phe35Leu
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30795
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe35Leu
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

12-10462229-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462229
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462229
    reference: chr 12
allele count: 3
allele frequency: 2.55306112028322e-5
allele num: 117506
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.145T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1903T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.105T>C
  hgvsp: ENST00000344825.6:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+150T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.105T>C
  hgvsp: ENST00000543420.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.12T>C
  hgvsp: ENST00000544747.1:c.12T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.105T>C
  hgvsp: ENST00000381907.4:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.12T>C
  hgvsp: ENST00000350274.5:c.12T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.105T>C
  hgvsp: ENST00000336164.4:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.105T>C
  hgvsp: ENST00000539374.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.105T>C
  hgvsp: ENST00000381908.3:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe35Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

12-10462240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462240
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462240
    reference: chr 12
allele count: 1
allele frequency: 8.435117079425063e-6
allele num: 118552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.116G>A
  hgvsp: ENSP00000344858.6:p.Ser39Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.23G>A
  hgvsp: ENSP00000310929.7:p.Ser8Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.116G>A
  hgvsp: ENSP00000371333.3:p.Ser39Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.116G>A
  hgvsp: ENSP00000371332.4:p.Ser39Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1914G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+161G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.116G>A
  hgvsp: ENSP00000441074.1:p.Ser39Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.116G>A
  hgvsp: ENSP00000438514.1:p.Ser39Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.156G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.116G>A
  hgvsp: ENSP00000338130.4:p.Ser39Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.23G>A
  hgvsp: ENSP00000438669.1:p.Ser8Asn
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser39Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

12-10462247-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462247
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462247
    reference: chr 12
allele count: 18
allele frequency: 1.51494748182063e-4
allele num: 118816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.123G>A
  hgvsp: ENST00000344825.6:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.163G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.123G>A
  hgvsp: ENST00000381907.4:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.123G>A
  hgvsp: ENST00000381908.3:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.123G>A
  hgvsp: ENST00000336164.4:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+168G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1921G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.123G>A
  hgvsp: ENST00000543420.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.123G>A
  hgvsp: ENST00000539374.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.30G>A
  hgvsp: ENST00000544747.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.30G>A
  hgvsp: ENST00000350274.5:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14583
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32631
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu41Glu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

12-10462248-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462248
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462248
    reference: chr 12
allele count: 1
allele frequency: 8.415808254224735e-6
allele num: 118824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+169C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.124C>T
  hgvsp: ENSP00000371333.3:p.Pro42Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.124C>T
  hgvsp: ENSP00000338130.4:p.Pro42Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.124C>T
  hgvsp: ENSP00000344858.6:p.Pro42Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1922C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.31C>T
  hgvsp: ENSP00000310929.7:p.Pro11Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.31C>T
  hgvsp: ENSP00000438669.1:p.Pro11Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.124C>T
  hgvsp: ENSP00000441074.1:p.Pro42Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.124C>T
  hgvsp: ENSP00000371332.4:p.Pro42Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.164C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.124C>T
  hgvsp: ENSP00000438514.1:p.Pro42Ser
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro42Ser
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

12-10462255-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462255
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462255
    reference: chr 12
allele count: 1
allele frequency: 8.40745909771149e-6
allele num: 118942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.131T>C
  hgvsp: ENSP00000344858.6:p.Phe44Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.131T>C
  hgvsp: ENSP00000438514.1:p.Phe44Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.131T>C
  hgvsp: ENSP00000371333.3:p.Phe44Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.131T>C
  hgvsp: ENSP00000371332.4:p.Phe44Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1929T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.131T>C
  hgvsp: ENSP00000338130.4:p.Phe44Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.131T>C
  hgvsp: ENSP00000441074.1:p.Phe44Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.38T>C
  hgvsp: ENSP00000438669.1:p.Phe13Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.171T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+176T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.38T>C
  hgvsp: ENSP00000310929.7:p.Phe13Ser
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14850
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe44Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

12-10462262-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462262
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462262
    reference: chr 12
allele count: 9
allele frequency: 7.57295277843223e-5
allele num: 118844
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.45A>G
  hgvsp: ENST00000350274.5:c.45A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.138A>G
  hgvsp: ENST00000344825.6:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1936A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.138A>G
  hgvsp: ENST00000539374.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.138A>G
  hgvsp: ENST00000381908.3:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.138A>G
  hgvsp: ENST00000543420.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.178A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+183A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.138A>G
  hgvsp: ENST00000381907.4:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.45A>G
  hgvsp: ENST00000544747.1:c.45A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.138A>G
  hgvsp: ENST00000336164.4:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15015
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro46Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

12-10462264-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462264
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462264
    reference: chr 12
allele count: 1
allele frequency: 8.412693071305987e-6
allele num: 118868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.180G>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.140G>C
  hgvsp: ENSP00000441074.1:p.Gly47Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.140G>C
  hgvsp: ENSP00000371333.3:p.Gly47Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.140G>C
  hgvsp: ENSP00000344858.6:p.Gly47Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.140G>C
  hgvsp: ENSP00000338130.4:p.Gly47Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.47G>C
  hgvsp: ENSP00000438669.1:p.Gly16Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1938G>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+185G>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.47G>C
  hgvsp: ENSP00000310929.7:p.Gly16Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.140G>C
  hgvsp: ENSP00000438514.1:p.Gly47Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.140G>C
  hgvsp: ENSP00000371332.4:p.Gly47Ala
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly47Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-10462267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462267
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462267
    reference: chr 12
allele count: 12
allele frequency: 1.010509296685529e-4
allele num: 118752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.143C>T
  hgvsp: ENSP00000441074.1:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.143C>T
  hgvsp: ENSP00000344858.6:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.143C>T
  hgvsp: ENSP00000371333.3:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.183C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.143C>T
  hgvsp: ENSP00000338130.4:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.143C>T
  hgvsp: ENSP00000438514.1:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1941C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.50C>T
  hgvsp: ENSP00000310929.7:p.Pro17Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.143C>T
  hgvsp: ENSP00000371332.4:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.50C>T
  hgvsp: ENSP00000438669.1:p.Pro17Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+188C>T
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15145
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro48Leu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

12-10462272-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462272
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462272
    reference: chr 12
allele count: 1
allele frequency: 8.441525552497847e-6
allele num: 118462
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.148A>G
  hgvsp: ENSP00000338130.4:p.Ile50Val
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.55A>G
  hgvsp: ENSP00000438669.1:p.Ile19Val
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.148A>G
  hgvsp: ENSP00000371332.4:p.Ile50Val
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.148A>G
  hgvsp: ENSP00000344858.6:p.Ile50Val
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.55A>G
  hgvsp: ENSP00000310929.7:p.Ile19Val
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.148A>G
  hgvsp: ENSP00000438514.1:p.Ile50Val
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.148A>G
  hgvsp: ENSP00000441074.1:p.Ile50Val
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+193A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.148A>G
  hgvsp: ENSP00000371333.3:p.Ile50Val
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1946A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.188A>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile50Val
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

12-10462288-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462288
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462288
    reference: chr 12
allele count: 1
allele frequency: 8.556955093099671e-6
allele num: 116864
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.70+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.203+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.70+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.163+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.163+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.163+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.163+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1961+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.163+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+209G>T
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15133
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: c.163+1G>T
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

12-10462295-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462295
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462295
    reference: chr 12
allele count: 1
allele frequency: 8.653812869950501e-6
allele num: 115556
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.70+8A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+216A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.163+8A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.163+8A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.70+8A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.163+8A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1961+8A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.203+8A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.163+8A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+8A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.163+8A>T
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26290
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.163+8A>T
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/12-10462308-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462308
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462308
    reference: chr 12
allele count: 3
allele frequency: 2.645222727753677e-5
allele num: 113412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1961+21A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.163+21A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.163+21A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.203+21A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+21A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.70+21A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.163+21A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.163+21A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.70+21A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+229A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.163+21A>C
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19273
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12654
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

12-10462314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462314
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462314
    reference: chr 12
allele count: 4
allele frequency: 3.564299971485601e-5
allele num: 112224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.163+27G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.70+27G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.163+27G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+27G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.163+27G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.203+27G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1961+27G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.163+27G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.70+27G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+235G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.163+27G>A
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10893
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

12-10462316-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462316
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462316
    reference: chr 12
allele count: 2
allele frequency: 1.785267968722105e-5
allele num: 112028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.163+29A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.163+29A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.163+29A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.163+29A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1961+29A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.203+29A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.163+29A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+237A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.70+29A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+29A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.70+29A>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13860
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6593
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

12-10462320-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462320
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462320
    reference: chr 12
allele count: 1
allele frequency: 8.995070701255712e-6
allele num: 111172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.163+33G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.203+33G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+33G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.70+33G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+241G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.163+33G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.163+33G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.163+33G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.70+33G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1961+33G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.163+33G>T
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4234
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

12-10462321-TAAAAGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462321
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462315
    reference: chr 12
allele count: 9
allele frequency: 8.140818061761673e-5
allele num: 110554
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.163+35_163+40delAAAAGA
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.163+35_163+40delAAAAGA
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.163+35_163+40delAAAAGA
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1961+35_1961+40delAAAAGA
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+243_100+248delAAAAGA
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.163+35_163+40delAAAAGA
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.70+35_70+40delAAAAGA
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.163+35_163+40delAAAAGA
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.203+35_203+40delAAAAGA
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.70+35_70+40delAAAAGA
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+35_163+40delAAAAGA
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16138
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11358
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4242
  bin: 9.75e1
  variant carriers: 9
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: TAAAAGA
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

12-10462329-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10462329
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10462329
    reference: chr 12
allele count: 3
allele frequency: 2.766710934041611e-5
allele num: 108432
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.70+42T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.163+42T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.100+250T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1961+42T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.70+42T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.203+42T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+42T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.163+42T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.163+42T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.163+42T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.163+42T>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7869
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4484
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/12-10464012-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464012
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464012
    reference: chr 12
allele count: 1
allele frequency: 8.334166750008334e-6
allele num: 119988
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1962-51A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.164-51A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.164-51A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.71-51A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.164-51A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.101-51A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.164-51A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.204-51A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.164-51A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.71-51A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1725A>C
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
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: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/12-10464015-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464015
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464015
    reference: chr 12
allele count: 1
allele frequency: 8.332777814812346e-6
allele num: 120008
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.204-48A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.164-48A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.164-48A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.71-48A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.101-48A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.164-48A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1728A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.164-48A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1962-48A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.164-48A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.71-48A>C
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

12-10464017-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464017
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464017
    reference: chr 12
allele count: 7740
allele frequency: 6.446239693512118e-2
allele num: 120070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.164-46T>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1962-46T>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.71-46T>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.101-46T>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.164-46T>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.204-46T>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.164-46T>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.71-46T>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.164-46T>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1730T>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.164-46T>A
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10978
  bin: 3.25e1
  variant carriers: 1018
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 1.25e1
  variant carriers: 196
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 3.75e1
  variant carriers: 1032
genotype depth: GenotypeDepth
  all individuals: 11286
  bin: 2.25e1
  variant carriers: 614
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 23092
  bin: 2.75e1
  variant carriers: 874
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 151
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 4.25e1
  variant carriers: 904
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.75e1
  variant carriers: 393
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.75e1
  variant carriers: 637
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 425
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 1.75e1
  variant carriers: 411
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 236
genotype quality: GenotypeQuality
  all individuals: 1094
  bin: 8.25e1
  variant carriers: 21
num of homozygotes: 313
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

12-10464018-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464018
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464018
    reference: chr 12
allele count: 1
allele frequency: 8.328058896032513e-6
allele num: 120076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.164-45G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.204-45G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.164-45G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.71-45G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.164-45G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.101-45G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.71-45G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.164-45G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.164-45G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1962-45G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1731G>A
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

12-10464027-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464027
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464027
    reference: chr 12
allele count: 1
allele frequency: 8.310755780130645e-6
allele num: 120326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.204-36C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.71-36C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.101-36C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1740C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.164-36C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.164-36C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.71-36C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1962-36C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.164-36C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.164-36C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.164-36C>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

12-10464027-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464027
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464027
    reference: chr 12
allele count: 1
allele frequency: 8.310755780130645e-6
allele num: 120326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1740C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.101-36C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.71-36C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.204-36C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1962-36C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.71-36C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.164-36C>T
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ

12-10464049-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464049
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464049
    reference: chr 12
allele count: 1
allele frequency: 8.269656974628692e-6
allele num: 120924
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.164-14A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.71-14A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.101-14A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.204-14A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.71-14A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1762A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.164-14A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.164-14A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.164-14A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1962-14A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.164-14A>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

12-10464065-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464065
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464065
    reference: chr 12
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1778T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.73T>G
  hgvsp: ENSP00000310929.7:p.Ser25Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.73T>G
  hgvsp: ENSP00000438669.1:p.Ser25Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.103T>G
  hgvsp: ENSP00000443584.1:p.Ser35Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.166T>G
  hgvsp: ENSP00000371332.4:p.Ser56Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.166T>G
  hgvsp: ENSP00000441074.1:p.Ser56Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.166T>G
  hgvsp: ENSP00000338130.4:p.Ser56Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.166T>G
  hgvsp: ENSP00000371333.3:p.Ser56Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.206T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.166T>G
  hgvsp: ENSP00000438514.1:p.Ser56Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1964T>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15263
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11737
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser56Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

12-10464066-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464066
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464066
    reference: chr 12
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.167C>T
  hgvsp: ENSP00000441074.1:p.Ser56Phe
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.167C>T
  hgvsp: ENSP00000371332.4:p.Ser56Phe
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.74C>T
  hgvsp: ENSP00000438669.1:p.Ser25Phe
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.167C>T
  hgvsp: ENSP00000338130.4:p.Ser56Phe
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1965C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.167C>T
  hgvsp: ENSP00000438514.1:p.Ser56Phe
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.167C>T
  hgvsp: ENSP00000371333.3:p.Ser56Phe
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.104C>T
  hgvsp: ENSP00000443584.1:p.Ser35Phe
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.74C>T
  hgvsp: ENSP00000310929.7:p.Ser25Phe
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.207C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1779C>T
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser56Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-10464078-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464078
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464078
    reference: chr 12
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1977C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.86C>A
  hgvsp: ENSP00000438669.1:p.Ser29Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.86C>A
  hgvsp: ENSP00000310929.7:p.Ser29Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.179C>A
  hgvsp: ENSP00000371332.4:p.Ser60Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.179C>A
  hgvsp: ENSP00000438514.1:p.Ser60Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.179C>A
  hgvsp: ENSP00000338130.4:p.Ser60Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.179C>A
  hgvsp: ENSP00000441074.1:p.Ser60Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.116C>A
  hgvsp: ENSP00000443584.1:p.Ser39Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.179C>A
  hgvsp: ENSP00000371333.3:p.Ser60Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.219C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1791C>A
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser60Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

12-10464082-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464082
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464082
    reference: chr 12
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.183C>G
  hgvsp: ENSP00000371332.4:p.Cys61Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1795C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.183C>G
  hgvsp: ENSP00000371333.3:p.Cys61Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.183C>G
  hgvsp: ENSP00000441074.1:p.Cys61Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.223C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1981C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.183C>G
  hgvsp: ENSP00000338130.4:p.Cys61Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.183C>G
  hgvsp: ENSP00000438514.1:p.Cys61Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.120C>G
  hgvsp: ENSP00000443584.1:p.Cys40Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.90C>G
  hgvsp: ENSP00000310929.7:p.Cys30Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.90C>G
  hgvsp: ENSP00000438669.1:p.Cys30Trp
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys61Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-10464096-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464096
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464096
    reference: chr 12
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.134T>G
  hgvsp: ENSP00000443584.1:p.Val45Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.197T>G
  hgvsp: ENSP00000338130.4:p.Val66Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.197T>G
  hgvsp: ENSP00000438514.1:p.Val66Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1809T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.104T>G
  hgvsp: ENSP00000438669.1:p.Val35Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.197T>G
  hgvsp: ENSP00000371333.3:p.Val66Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.197T>G
  hgvsp: ENSP00000371332.4:p.Val66Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.197T>G
  hgvsp: ENSP00000441074.1:p.Val66Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1995T>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.104T>G
  hgvsp: ENSP00000310929.7:p.Val35Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.237T>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val66Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-10464099-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464099
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464099
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.200G>A
  hgvsp: ENSP00000371333.3:p.Gly67Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.240G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.107G>A
  hgvsp: ENSP00000438669.1:p.Gly36Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.137G>A
  hgvsp: ENSP00000443584.1:p.Gly46Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.1998G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.200G>A
  hgvsp: ENSP00000338130.4:p.Gly67Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.107G>A
  hgvsp: ENSP00000310929.7:p.Gly36Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1812G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.200G>A
  hgvsp: ENSP00000441074.1:p.Gly67Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.200G>A
  hgvsp: ENSP00000371332.4:p.Gly67Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.200G>A
  hgvsp: ENSP00000438514.1:p.Gly67Glu
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly67Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

12-10464104-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464104
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464104
    reference: chr 12
allele count: 18
allele frequency: 1.48294611962432e-4
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.205C>T
  hgvsp: ENSP00000338130.4:p.Arg69Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.245C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1817C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.205C>T
  hgvsp: ENSP00000441074.1:p.Arg69Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.112C>T
  hgvsp: ENSP00000438669.1:p.Arg38Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.205C>T
  hgvsp: ENSP00000371332.4:p.Arg69Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.112C>T
  hgvsp: ENSP00000310929.7:p.Arg38Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.142C>T
  hgvsp: ENSP00000443584.1:p.Arg48Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.205C>T
  hgvsp: ENSP00000438514.1:p.Arg69Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.205C>T
  hgvsp: ENSP00000371333.3:p.Arg69Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2003C>T
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg69Trp
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

12-10464105-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464105
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464105
    reference: chr 12
allele count: 10
allele frequency: 8.238453806989504e-5
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.206G>A
  hgvsp: ENSP00000371333.3:p.Arg69Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.206G>A
  hgvsp: ENSP00000438514.1:p.Arg69Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.206G>A
  hgvsp: ENSP00000371332.4:p.Arg69Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2004G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.143G>A
  hgvsp: ENSP00000443584.1:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.246G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.206G>A
  hgvsp: ENSP00000441074.1:p.Arg69Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.206G>A
  hgvsp: ENSP00000338130.4:p.Arg69Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.113G>A
  hgvsp: ENSP00000310929.7:p.Arg38Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.113G>A
  hgvsp: ENSP00000438669.1:p.Arg38Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1818G>A
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11780
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg69Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

12-10464105-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464105
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464105
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.143G>T
  hgvsp: ENSP00000443584.1:p.Arg48Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.206G>T
  hgvsp: ENSP00000338130.4:p.Arg69Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.206G>T
  hgvsp: ENSP00000438514.1:p.Arg69Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.113G>T
  hgvsp: ENSP00000438669.1:p.Arg38Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2004G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.206G>T
  hgvsp: ENSP00000441074.1:p.Arg69Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1818G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.246G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.206G>T
  hgvsp: ENSP00000371332.4:p.Arg69Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.206G>T
  hgvsp: ENSP00000371333.3:p.Arg69Leu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.113G>T
  hgvsp: ENSP00000310929.7:p.Arg38Leu
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg69Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS

12-10464114-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464114
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464114
    reference: chr 12
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.215G>A
  hgvsp: ENSP00000371332.4:p.Cys72Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.215G>A
  hgvsp: ENSP00000438514.1:p.Cys72Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2013G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.255G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1827G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.215G>A
  hgvsp: ENSP00000441074.1:p.Cys72Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.122G>A
  hgvsp: ENSP00000438669.1:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.215G>A
  hgvsp: ENSP00000338130.4:p.Cys72Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.215G>A
  hgvsp: ENSP00000371333.3:p.Cys72Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.122G>A
  hgvsp: ENSP00000310929.7:p.Cys41Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.152G>A
  hgvsp: ENSP00000443584.1:p.Cys51Tyr
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Cys72Tyr
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-10464117-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464117
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464117
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.218A>C
  hgvsp: ENSP00000338130.4:p.Tyr73Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.125A>C
  hgvsp: ENSP00000310929.7:p.Tyr42Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.155A>C
  hgvsp: ENSP00000443584.1:p.Tyr52Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1830A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.258A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.218A>C
  hgvsp: ENSP00000371332.4:p.Tyr73Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.218A>C
  hgvsp: ENSP00000438514.1:p.Tyr73Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.125A>C
  hgvsp: ENSP00000438669.1:p.Tyr42Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.218A>C
  hgvsp: ENSP00000441074.1:p.Tyr73Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.218A>C
  hgvsp: ENSP00000371333.3:p.Tyr73Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2016A>C
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr73Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

12-10464134-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464134
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464134
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.142C>G
  hgvsp: ENSP00000310929.7:p.Gln48Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1847C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2033C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.172C>G
  hgvsp: ENSP00000443584.1:p.Gln58Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.235C>G
  hgvsp: ENSP00000438514.1:p.Gln79Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.235C>G
  hgvsp: ENSP00000441074.1:p.Gln79Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.275C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.235C>G
  hgvsp: ENSP00000338130.4:p.Gln79Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.142C>G
  hgvsp: ENSP00000438669.1:p.Gln48Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.235C>G
  hgvsp: ENSP00000371332.4:p.Gln79Glu
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.235C>G
  hgvsp: ENSP00000371333.3:p.Gln79Glu
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln79Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

12-10464136-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464136
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464136
    reference: chr 12
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1849G>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.144G>C
  hgvsp: ENSP00000310929.7:p.Gln48His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.144G>C
  hgvsp: ENSP00000438669.1:p.Gln48His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.237G>C
  hgvsp: ENSP00000438514.1:p.Gln79His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.237G>C
  hgvsp: ENSP00000441074.1:p.Gln79His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.237G>C
  hgvsp: ENSP00000338130.4:p.Gln79His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.237G>C
  hgvsp: ENSP00000371333.3:p.Gln79His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.237G>C
  hgvsp: ENSP00000371332.4:p.Gln79His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.174G>C
  hgvsp: ENSP00000443584.1:p.Gln58His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2035G>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.277G>C
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln79His
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-10464138-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464138
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464138
    reference: chr 12
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.239A>G
  hgvsp: ENSP00000371332.4:p.Lys80Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.146A>G
  hgvsp: ENSP00000310929.7:p.Lys49Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1851A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.239A>G
  hgvsp: ENSP00000441074.1:p.Lys80Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.239A>G
  hgvsp: ENSP00000371333.3:p.Lys80Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.176A>G
  hgvsp: ENSP00000443584.1:p.Lys59Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.239A>G
  hgvsp: ENSP00000338130.4:p.Lys80Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.279A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.239A>G
  hgvsp: ENSP00000438514.1:p.Lys80Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2037A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.146A>G
  hgvsp: ENSP00000438669.1:p.Lys49Arg
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys80Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

12-10464140-ACTTG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464140
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464136
    reference: chr 12
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.149_152delCTTG
  hgvsp: ENSP00000438669.1:p.Thr50ArgfsTer27
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.242_245delCTTG
  hgvsp: ENSP00000338130.4:p.Thr81ArgfsTer27
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.282_285delCTTG
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.149_152delCTTG
  hgvsp: ENSP00000310929.7:p.Thr50ArgfsTer27
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.242_245delCTTG
  hgvsp: ENSP00000441074.1:p.Thr81ArgfsTer82
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.242_245delCTTG
  hgvsp: ENSP00000371332.4:p.Thr81ArgfsTer27
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.242_245delCTTG
  hgvsp: ENSP00000438514.1:p.Thr81ArgfsTer100
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.242_245delCTTG
  hgvsp: ENSP00000371333.3:p.Thr81ArgfsTer28
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.179_182delCTTG
  hgvsp: ENSP00000443584.1:p.Thr60ArgfsTer27
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1854_163+1857delCTTG
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2040_2043delCTTG
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr81ArgfsTer27
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: ACTTG
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

12-10464142-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464142
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464142
    reference: chr 12
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.150T>C
  hgvsp: ENST00000544747.1:c.150T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.243T>C
  hgvsp: ENST00000381907.4:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.243T>C
  hgvsp: ENST00000539374.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.163+1855T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2041T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.180T>C
  hgvsp: ENST00000543777.1:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.243T>C
  hgvsp: ENST00000336164.4:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.243T>C
  hgvsp: ENST00000543420.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.243T>C
  hgvsp: ENST00000381908.3:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.283T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.150T>C
  hgvsp: ENST00000350274.5:c.150T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr81Thr
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

12-10464148-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464148
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464148
    reference: chr 12
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.249C>G
  hgvsp: ENSP00000338130.4:p.Asn83Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.249C>G
  hgvsp: ENSP00000371332.4:p.Asn83Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2047C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.156C>G
  hgvsp: ENSP00000310929.7:p.Asn52Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.249C>G
  hgvsp: ENSP00000371333.3:p.Asn83Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.156C>G
  hgvsp: ENSP00000438669.1:p.Asn52Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.249C>G
  hgvsp: ENSP00000438514.1:p.Asn83Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.249C>G
  hgvsp: ENSP00000441074.1:p.Asn83Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.289C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.186C>G
  hgvsp: ENSP00000443584.1:p.Asn62Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1858C>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn83Lys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

12-10464148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464148
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464148
    reference: chr 12
allele count: 3
allele frequency: 2.47161759132627e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.249C>T
  hgvsp: ENST00000336164.4:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1858C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.156C>T
  hgvsp: ENST00000544747.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.156C>T
  hgvsp: ENST00000350274.5:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.186C>T
  hgvsp: ENST00000543777.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2047C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.249C>T
  hgvsp: ENST00000543420.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.249C>T
  hgvsp: ENST00000381907.4:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.289C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.249C>T
  hgvsp: ENST00000381908.3:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.249C>T
  hgvsp: ENST00000539374.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  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: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn83Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

12-10464149-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464149
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464149
    reference: chr 12
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.290G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.250G>A
  hgvsp: ENSP00000371333.3:p.Glu84Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2048G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.250G>A
  hgvsp: ENSP00000338130.4:p.Glu84Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.250G>A
  hgvsp: ENSP00000438514.1:p.Glu84Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.250G>A
  hgvsp: ENSP00000441074.1:p.Glu84Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.250G>A
  hgvsp: ENSP00000371332.4:p.Glu84Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.157G>A
  hgvsp: ENSP00000438669.1:p.Glu53Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.157G>A
  hgvsp: ENSP00000310929.7:p.Glu53Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.187G>A
  hgvsp: ENSP00000443584.1:p.Glu63Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1857G>A
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu84Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

http://identifiers.org/exac.variant/12-10464150-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464150
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464150
    reference: chr 12
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.158A>C
  hgvsp: ENSP00000438669.1:p.Glu53Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.251A>C
  hgvsp: ENSP00000338130.4:p.Glu84Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.251A>C
  hgvsp: ENSP00000371332.4:p.Glu84Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.251A>C
  hgvsp: ENSP00000438514.1:p.Glu84Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.291A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.251A>C
  hgvsp: ENSP00000441074.1:p.Glu84Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.158A>C
  hgvsp: ENSP00000310929.7:p.Glu53Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2049A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1856A>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.251A>C
  hgvsp: ENSP00000371333.3:p.Glu84Ala
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.188A>C
  hgvsp: ENSP00000443584.1:p.Glu63Ala
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu84Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

12-10464150-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464150
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464150
    reference: chr 12
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1856A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.251A>G
  hgvsp: ENSP00000338130.4:p.Glu84Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.251A>G
  hgvsp: ENSP00000371332.4:p.Glu84Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.251A>G
  hgvsp: ENSP00000441074.1:p.Glu84Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2049A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.188A>G
  hgvsp: ENSP00000443584.1:p.Glu63Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.251A>G
  hgvsp: ENSP00000438514.1:p.Glu84Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.251A>G
  hgvsp: ENSP00000371333.3:p.Glu84Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.158A>G
  hgvsp: ENSP00000310929.7:p.Glu53Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.158A>G
  hgvsp: ENSP00000438669.1:p.Glu53Gly
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.291A>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu84Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

12-10464152-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464152
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464152
    reference: chr 12
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.160A>T
  hgvsp: ENSP00000310929.7:p.Ser54Cys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.293A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.253A>T
  hgvsp: ENSP00000438514.1:p.Ser85Cys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.190A>T
  hgvsp: ENSP00000443584.1:p.Ser64Cys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2051A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.253A>T
  hgvsp: ENSP00000441074.1:p.Ser85Cys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.160A>T
  hgvsp: ENSP00000438669.1:p.Ser54Cys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.253A>T
  hgvsp: ENSP00000371332.4:p.Ser85Cys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.253A>T
  hgvsp: ENSP00000338130.4:p.Ser85Cys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1854A>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.253A>T
  hgvsp: ENSP00000371333.3:p.Ser85Cys
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser85Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

12-10464155-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464155
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464155
    reference: chr 12
allele count: 7
allele frequency: 5.767202741892961e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.163C>T
  hgvsp: ENSP00000310929.7:p.Arg55Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1851C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.296C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.256C>T
  hgvsp: ENSP00000371333.3:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.256C>T
  hgvsp: ENSP00000441074.1:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.163C>T
  hgvsp: ENSP00000438669.1:p.Arg55Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2054C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.256C>T
  hgvsp: ENSP00000371332.4:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.256C>T
  hgvsp: ENSP00000438514.1:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.256C>T
  hgvsp: ENSP00000338130.4:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.193C>T
  hgvsp: ENSP00000443584.1:p.Arg65Trp
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg86Trp
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-10464156-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464156
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464156
    reference: chr 12
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.164G>A
  hgvsp: ENSP00000310929.7:p.Arg55Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.257G>A
  hgvsp: ENSP00000441074.1:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.164G>A
  hgvsp: ENSP00000438669.1:p.Arg55Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.257G>A
  hgvsp: ENSP00000438514.1:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.257G>A
  hgvsp: ENSP00000338130.4:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.257G>A
  hgvsp: ENSP00000371332.4:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.297G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.257G>A
  hgvsp: ENSP00000371333.3:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.194G>A
  hgvsp: ENSP00000443584.1:p.Arg65Gln
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2055G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1850G>A
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg86Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-10464158-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464158
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464158
    reference: chr 12
allele count: 10
allele frequency: 8.239132584121544e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1848C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.166C>A
  hgvsp: ENSP00000438669.1:p.His56Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.166C>A
  hgvsp: ENSP00000310929.7:p.His56Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.259C>A
  hgvsp: ENSP00000441074.1:p.His87Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.299C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.259C>A
  hgvsp: ENSP00000371332.4:p.His87Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.259C>A
  hgvsp: ENSP00000338130.4:p.His87Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.259C>A
  hgvsp: ENSP00000438514.1:p.His87Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.259C>A
  hgvsp: ENSP00000371333.3:p.His87Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.196C>A
  hgvsp: ENSP00000443584.1:p.His66Asn
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2057C>A
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His87Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

12-10464159-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464159
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464159
    reference: chr 12
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.260A>G
  hgvsp: ENSP00000371332.4:p.His87Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.260A>G
  hgvsp: ENSP00000371333.3:p.His87Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1847A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.167A>G
  hgvsp: ENSP00000310929.7:p.His56Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.260A>G
  hgvsp: ENSP00000441074.1:p.His87Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.260A>G
  hgvsp: ENSP00000338130.4:p.His87Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.167A>G
  hgvsp: ENSP00000438669.1:p.His56Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.197A>G
  hgvsp: ENSP00000443584.1:p.His66Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.300A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2058A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.260A>G
  hgvsp: ENSP00000438514.1:p.His87Arg
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His87Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/12-10464180-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464180
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464180
    reference: chr 12
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.281C>A
  hgvsp: ENSP00000438514.1:p.Ser94Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.281C>A
  hgvsp: ENSP00000441074.1:p.Ser94Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.188C>A
  hgvsp: ENSP00000310929.7:p.Ser63Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2079C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1826C>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.281C>A
  hgvsp: ENSP00000371333.3:p.Ser94Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.281C>A
  hgvsp: ENSP00000371332.4:p.Ser94Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.218C>A
  hgvsp: ENSP00000443584.1:p.Ser73Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.281C>A
  hgvsp: ENSP00000338130.4:p.Ser94Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.188C>A
  hgvsp: ENSP00000438669.1:p.Ser63Tyr
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.321C>A
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser94Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

12-10464183-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464183
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464184
    reference: chr 12
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.286dupC
  hgvsp: ENSP00000441074.1:p.Leu96ProfsTer9
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1821dupC
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.326dupC
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.286dupC
  hgvsp: ENSP00000438514.1:p.Leu96ProfsTer9
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.223dupC
  hgvsp: ENSP00000443584.1:p.Leu75ProfsTer9
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.193dupC
  hgvsp: ENSP00000310929.7:p.Leu65ProfsTer9
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.286dupC
  hgvsp: ENSP00000338130.4:p.Leu96ProfsTer9
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.286dupC
  hgvsp: ENSP00000371332.4:p.Leu96ProfsTer9
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.286dupC
  hgvsp: ENSP00000371333.3:p.Leu96ProfsTer9
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.193dupC
  hgvsp: ENSP00000438669.1:p.Leu65ProfsTer9
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2084dupC
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu96ProfsTer9
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

12-10464202-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464202
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464202
    reference: chr 12
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.303C>G
  hgvsp: ENSP00000438514.1:p.Asn101Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1804C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.303C>G
  hgvsp: ENSP00000371333.3:p.Asn101Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.303C>G
  hgvsp: ENSP00000338130.4:p.Asn101Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.240C>G
  hgvsp: ENSP00000443584.1:p.Asn80Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2101C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.303C>G
  hgvsp: ENSP00000441074.1:p.Asn101Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.210C>G
  hgvsp: ENSP00000438669.1:p.Asn70Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.210C>G
  hgvsp: ENSP00000310929.7:p.Asn70Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.303C>G
  hgvsp: ENSP00000371332.4:p.Asn101Lys
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.343C>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn101Lys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

12-10464202-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464202
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464202
    reference: chr 12
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.210C>T
  hgvsp: ENST00000544747.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.303C>T
  hgvsp: ENST00000543420.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1804C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.303C>T
  hgvsp: ENST00000381907.4:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.210C>T
  hgvsp: ENST00000350274.5:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.303C>T
  hgvsp: ENST00000336164.4:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.240C>T
  hgvsp: ENST00000543777.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2101C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.303C>T
  hgvsp: ENST00000381908.3:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.343C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.303C>T
  hgvsp: ENST00000539374.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn101Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

12-10464204-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464204
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464204
    reference: chr 12
allele count: 7
allele frequency: 5.777579689331286e-5
allele num: 121158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.305C>T
  hgvsp: ENSP00000371333.3:p.Thr102Ile
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.305C>T
  hgvsp: ENSP00000438514.1:p.Thr102Ile
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.305C>T
  hgvsp: ENSP00000338130.4:p.Thr102Ile
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2103C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.305C>T
  hgvsp: ENSP00000371332.4:p.Thr102Ile
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1802C>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.305C>T
  hgvsp: ENSP00000441074.1:p.Thr102Ile
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.212C>T
  hgvsp: ENSP00000310929.7:p.Thr71Ile
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.242C>T
  hgvsp: ENSP00000443584.1:p.Thr81Ile
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.212C>T
  hgvsp: ENSP00000438669.1:p.Thr71Ile
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.345C>T
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr102Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

12-10464204-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464204
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464204
    reference: chr 12
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.345C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.305C>G
  hgvsp: ENSP00000441074.1:p.Thr102Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.305C>G
  hgvsp: ENSP00000371332.4:p.Thr102Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.212C>G
  hgvsp: ENSP00000438669.1:p.Thr71Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.305C>G
  hgvsp: ENSP00000338130.4:p.Thr102Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2103C>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.305C>G
  hgvsp: ENSP00000438514.1:p.Thr102Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.305C>G
  hgvsp: ENSP00000371333.3:p.Thr102Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.242C>G
  hgvsp: ENSP00000443584.1:p.Thr81Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.212C>G
  hgvsp: ENSP00000310929.7:p.Thr71Arg
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1802C>G
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr102Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

12-10464206-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464206
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464206
    reference: chr 12
allele count: 5
allele frequency: 4.128955539406752e-5
allele num: 121096
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.307G>C
  hgvsp: ENSP00000338130.4:p.Asp103His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.347G>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.307G>C
  hgvsp: ENSP00000441074.1:p.Asp103His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.214G>C
  hgvsp: ENSP00000438669.1:p.Asp72His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.307G>C
  hgvsp: ENSP00000371333.3:p.Asp103His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2105G>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1800G>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.307G>C
  hgvsp: ENSP00000438514.1:p.Asp103His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.214G>C
  hgvsp: ENSP00000310929.7:p.Asp72His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.307G>C
  hgvsp: ENSP00000371332.4:p.Asp103His
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.244G>C
  hgvsp: ENSP00000443584.1:p.Asp82His
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27612
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp103His
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

12-10464209-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464209
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464209
    reference: chr 12
allele count: 2
allele frequency: 1.652974527662529e-5
allele num: 120994
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.310G>T
  hgvsp: ENSP00000338130.4:p.Glu104Ter
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.310G>T
  hgvsp: ENSP00000371332.4:p.Glu104Ter
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.310G>T
  hgvsp: ENSP00000371333.3:p.Glu104Ter
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.310G>T
  hgvsp: ENSP00000438514.1:p.Glu104Ter
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1797G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.217G>T
  hgvsp: ENSP00000310929.7:p.Glu73Ter
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.310G>T
  hgvsp: ENSP00000441074.1:p.Glu104Ter
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.217G>T
  hgvsp: ENSP00000438669.1:p.Glu73Ter
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.350G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2108G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.247G>T
  hgvsp: ENSP00000443584.1:p.Glu83Ter
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11689
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu104Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

12-10464211-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464211
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464211
    reference: chr 12
allele count: 1
allele frequency: 8.267195767195768e-6
allele num: 120960
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1795A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.312A>G
  hgvsp: ENST00000543420.1:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.352A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2110A>G
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.312A>G
  hgvsp: ENST00000539374.1:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.219A>G
  hgvsp: ENST00000350274.5:c.219A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.312A>G
  hgvsp: ENST00000336164.4:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.249A>G
  hgvsp: ENST00000543777.1:c.249A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.219A>G
  hgvsp: ENST00000544747.1:c.219A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.312A>G
  hgvsp: ENST00000381907.4:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.312A>G
  hgvsp: ENST00000381908.3:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu104Glu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum

12-10464214-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464214
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464214
    reference: chr 12
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.315G>A
  hgvsp: ENST00000336164.4:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.315G>A
  hgvsp: ENST00000539374.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2113G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1792G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.315G>A
  hgvsp: ENST00000381907.4:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.222G>A
  hgvsp: ENST00000350274.5:c.222G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.222G>A
  hgvsp: ENST00000544747.1:c.222G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.315G>A
  hgvsp: ENST00000381908.3:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.355G>A
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.315G>A
  hgvsp: ENST00000543420.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.252G>A
  hgvsp: ENST00000543777.1:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.315G>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

12-10464215-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464215
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464215
    reference: chr 12
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1791G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2113+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.252+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.316G>T
  hgvsp: ENSP00000438514.1:p.Ala106Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.315+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.356G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.316G>T
  hgvsp: ENSP00000441074.1:p.Ala106Ser
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.315+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.315+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.222+1G>T
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.222+1G>T
  variant of: http://identifiers.org/hgnc/6378
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.315+1G>T
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

12-10464220-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10464220
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 10464220
    reference: chr 12
allele count: 1
allele frequency: 8.311861025683651e-6
allele num: 120310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000310929
  ensembl transcript: ENST00000350274
  gene symbol: KLRD1
  hgvsc: ENST00000350274.5:c.222+6T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000344858
  ensembl transcript: ENST00000344825
  gene symbol: KLRD1
  hgvsc: ENST00000344825.6:c.164-1786T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371333
  ensembl transcript: ENST00000381908
  gene symbol: KLRD1
  hgvsc: ENST00000381908.3:c.315+6T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000338130
  ensembl transcript: ENST00000336164
  gene symbol: KLRD1
  hgvsc: ENST00000336164.4:c.315+6T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000538997
  gene symbol: KLRD1
  hgvsc: ENST00000538997.1:n.361T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000441074
  ensembl transcript: ENST00000543420
  gene symbol: KLRD1
  hgvsc: ENST00000543420.1:c.319+2T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438514
  ensembl transcript: ENST00000539374
  gene symbol: KLRD1
  hgvsc: ENST00000539374.1:c.319+2T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000443584
  ensembl transcript: ENST00000543777
  gene symbol: KLRD1
  hgvsc: ENST00000543777.1:c.252+6T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000371332
  ensembl transcript: ENST00000381907
  gene symbol: KLRD1
  hgvsc: ENST00000381907.4:c.315+6T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl transcript: ENST00000540271
  gene symbol: KLRD1
  hgvsc: ENST00000540271.1:n.2113+6T>C
  variant of: http://identifiers.org/hgnc/6378
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134539
  ensembl protein: ENSP00000438669
  ensembl transcript: ENST00000544747
  gene symbol: KLRD1
  hgvsc: ENST00000544747.1:c.222+6T>C
  variant of: http://identifiers.org/hgnc/6378
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.319+2T>C
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 318
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3961
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3714
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2788
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1540
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3135
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10842
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3171
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5639
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2211
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.75377060680463e-4
allele num: 11404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.076790548855525e-4
allele num: 65008
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.049e0

VQSLOD
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 2.045471e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.529e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.887e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.35e-1

GenotypeQuality
all individuals: 340
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2517
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3213
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1127
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4247
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4980
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4728
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22556
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.360513929525506e-5
allele num: 15722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7726
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11028
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

DP
type: SiteQuality
SIO_000300: 1.416998e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 2.636e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.366e-1

GenotypeQuality
all individuals: 174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1924
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3192
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5111
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31294
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1085
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4248
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1029
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61820
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.944543828264758e-5
allele num: 11180
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7930
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9668
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 1.489284e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

MQRankSum
type: SiteQuality
SIO_000300: -5.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.301e1

GenotypeQuality
all individuals: 3375
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 926
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.609321188322765e-5
allele num: 62138
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15866
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11224
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

DP
type: SiteQuality
SIO_000300: 1.502701e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.97e0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

QD
type: SiteQuality
SIO_000300: 1.747e1

FS
type: SiteQuality
SIO_000300: 3.081e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeDepth
all individuals: 168
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39553
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variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 978
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GenotypeQuality
all individuals: 201
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GenotypeQuality
all individuals: 424
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 19

GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 923
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 567
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variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3561
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15982
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.52112676056338e-4
allele num: 11360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 7.126858073712074e-4
allele num: 9822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.419782300047326e-4
allele num: 63390
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

QD
type: SiteQuality
SIO_000300: 1.509e1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.561296e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

FS
type: SiteQuality
SIO_000300: 1.153e0

GenotypeDepth
all individuals: 292
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 947
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 669
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variant carriers: 0

GenotypeQuality
all individuals: 1136
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variant carriers: 0

GenotypeQuality
all individuals: 1123
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variant carriers: 0

GenotypeQuality
all individuals: 1406
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 556
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variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 915
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GenotypeQuality
all individuals: 4246
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variant carriers: 1

GenotypeQuality
all individuals: 424
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 63
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GenotypeQuality
all individuals: 570
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 865
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variant carriers: 0

GenotypeQuality
all individuals: 344
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variant carriers: 0

GenotypeQuality
all individuals: 2820
bin: 2.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562011871290222e-5
allele num: 64020
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.059e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

FS
type: SiteQuality
SIO_000300: 3.222e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

MQRankSum
type: SiteQuality
SIO_000300: -4.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

DP
type: SiteQuality
SIO_000300: 1.582201e6

GenotypeDepth
all individuals: 31244
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 462
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variant carriers: 0

GenotypeQuality
all individuals: 595
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GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1128
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variant carriers: 0

GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 4248
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
all individuals: 866
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GenotypeQuality
all individuals: 1407
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GenotypeQuality
all individuals: 787
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GenotypeQuality
all individuals: 347
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GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
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GenotypeQuality
all individuals: 569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3690
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.752541184717841e-4
allele num: 11412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557923599426684e-5
allele num: 64188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16110
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.205e-1

QD
type: SiteQuality
SIO_000300: 1.076e1

FS
type: SiteQuality
SIO_000300: 7.659e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.471e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e0

DP
type: SiteQuality
SIO_000300: 1.587483e6

GenotypeDepth
all individuals: 2187
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
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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
all individuals: 37
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 572
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GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 1884
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GenotypeQuality
all individuals: 4243
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variant carriers: 1

GenotypeQuality
all individuals: 1141
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541734759951898e-5
allele num: 64862
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16242
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.223e1

VQSLOD
type: SiteQuality
SIO_000300: -1.426e0

MQRankSum
type: SiteQuality
SIO_000300: -2.165e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.915e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 1.608772e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 3.485e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.79e-1

GenotypeDepth
all individuals: 117
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
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variant carriers: 0

GenotypeQuality
all individuals: 1693
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 1144
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GenotypeQuality
all individuals: 169
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GenotypeQuality
all individuals: 151
bin: 4.75e1
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GenotypeQuality
all individuals: 577
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GenotypeQuality
all individuals: 230
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GenotypeQuality
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GenotypeQuality
all individuals: 864
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 44432
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3810
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4259
bin: 9.75e1
variant carriers: 18

Latino
type: Population
allele count: 18
allele frequency: 1.569311246730602e-3
allele num: 11470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65028
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

DP
type: SiteQuality
SIO_000300: 1.615873e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

FS
type: SiteQuality
SIO_000300: 5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

BaseQRankSum
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SIO_000300: -1.511e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

QD
type: SiteQuality
SIO_000300: 1.087e1

GenotypeDepth
all individuals: 168
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 237
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GenotypeQuality
all individuals: 249
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GenotypeQuality
all individuals: 245
bin: 2.75e1
variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8308
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.586797841954935e-5
allele num: 63020
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
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FS
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: 3.35e0

DP
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QD
type: SiteQuality
SIO_000300: 8.07e0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 61772
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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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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East Asian
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allele frequency: 3.699136868064119e-4
allele num: 8110
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VQSLOD
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MQRankSum
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DP
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QD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 2.41e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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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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African
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allele frequency: 4.290924694271615e-4
allele num: 9322
num of homozygotes: 0

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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num of homozygotes: 0

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

Latino
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: -2.1e-3

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.280301787764474e-5
allele num: 60970
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8014
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.91e-1

DP
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QD
type: SiteQuality
SIO_000300: 1.29e1

InbreedingCoeff
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SIO_000300: -2.1e-3

MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.92e0

ReadPosRankSum
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SIO_000300: 1.46e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.48e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9226
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 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

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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ReadPosRankSum
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DP
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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SIO_000300: -1.869e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.637024913620658e-4
allele num: 10998
num of homozygotes: 0

South Asian
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6406
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African
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allele frequency: 0.0e0
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East Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 8.327504080477e-5
allele num: 60042
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BaseQRankSum
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FS
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MQ
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ClippingRankSum
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QD
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DP
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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Other
type: Population
allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 2.77623542476402e-4
allele num: 10806
num of homozygotes: 0

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

East Asian
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African
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.506341698550899e-5
allele num: 66386
num of homozygotes: 0

Latino
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Other
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MQRankSum
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SIO_000300: -1.54e-1

BaseQRankSum
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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SIO_000300: 2.872e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.778e0

GenotypeQuality
all individuals: 31596
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
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GenotypeQuality
all individuals: 6305
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1458
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8014
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1176
bin: 5.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506160195198361e-5
allele num: 66394
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.72e-1

QD
type: SiteQuality
SIO_000300: 1.364e1

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.71e-1

DP
type: SiteQuality
SIO_000300: 1.773835e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

MQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

GenotypeQuality
all individuals: 31779
bin: 6.25e1
variant carriers: 13

GenotypeQuality
all individuals: 9795
bin: 9.75e1
variant carriers: 7235

GenotypeQuality
all individuals: 454
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 218
bin: 5.75e1
variant carriers: 9

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 72
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 651
bin: 4.25e1
variant carriers: 13

GenotypeQuality
all individuals: 803
bin: 3.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1012
bin: 3.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1887
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variant carriers: 23

GenotypeQuality
all individuals: 445
bin: 8.75e1
variant carriers: 18

GenotypeQuality
all individuals: 595
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 582
bin: 9.25e1
variant carriers: 38

GenotypeQuality
all individuals: 1742
bin: 7.25e1
variant carriers: 15

GenotypeQuality
all individuals: 1123
bin: 4.75e1
variant carriers: 13

GenotypeQuality
all individuals: 727
bin: 5.25e1
variant carriers: 16

GenotypeQuality
all individuals: 7616
bin: 6.75e1
variant carriers: 31

African
type: Population
allele count: 420
allele frequency: 4.057971014492753e-2
allele num: 10350
num of homozygotes: 7

South Asian
type: Population
allele count: 1080
allele frequency: 6.892150606253988e-2
allele num: 15670
num of homozygotes: 45

Other
type: Population
allele count: 57
allele frequency: 6.333333333333334e-2
allele num: 900
num of homozygotes: 1

Latino
type: Population
allele count: 358
allele frequency: 3.098494028042236e-2
allele num: 11554
num of homozygotes: 9

East Asian
type: Population
allele count: 1501
allele frequency: 1.745348837209302e-1
allele num: 8600
num of homozygotes: 112

European (Non-Finnish)
type: Population
allele count: 3886
allele frequency: 5.853820197637985e-2
allele num: 66384
num of homozygotes: 123

European (Finnish)
type: Population
allele count: 438
allele frequency: 6.624319419237749e-2
allele num: 6612
num of homozygotes: 16

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

DP
type: SiteQuality
SIO_000300: 1.803086e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e-1

QD
type: SiteQuality
SIO_000300: 1.544e1

VQSLOD
type: SiteQuality
SIO_000300: 6.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 683
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 2120
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8704
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variant carriers: 0

GenotypeQuality
all individuals: 482
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variant carriers: 0

GenotypeQuality
all individuals: 628
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variant carriers: 0

GenotypeQuality
all individuals: 236
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variant carriers: 0

GenotypeQuality
all individuals: 2964
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variant carriers: 1

GenotypeQuality
all individuals: 1126
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variant carriers: 0

GenotypeQuality
all individuals: 36576
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variant carriers: 0

GenotypeQuality
all individuals: 1066
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
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variant carriers: 0

GenotypeQuality
all individuals: 2010
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variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505751972535084e-5
allele num: 66412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15638
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.283e0

MQRankSum
type: SiteQuality
SIO_000300: -8.4e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

DP
type: SiteQuality
SIO_000300: 1.69103e6

MQ
type: SiteQuality
SIO_000300: 5.908e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

GenotypeQuality
all individuals: 1195
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39634
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variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 388
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variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 620
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variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2952
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 558
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
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variant carriers: 0

GenotypeQuality
all individuals: 8843
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2097
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variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
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: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15782
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -9.933e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.027e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

FS
type: SiteQuality
SIO_000300: 1.1272e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.472e1

DP
type: SiteQuality
SIO_000300: 1.71055e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.06e-1

GenotypeQuality
all individuals: 620
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 240
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variant carriers: 0

GenotypeQuality
all individuals: 8843
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variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 39634
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2952
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2097
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 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: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15782
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
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: 1.504302304591131e-5
allele num: 66476
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.933e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.027e0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 1.472e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.18e-1

FS
type: SiteQuality
SIO_000300: 1.1272e1

DP
type: SiteQuality
SIO_000300: 1.71055e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 287
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 130
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variant carriers: 0

GenotypeQuality
all individuals: 1200
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variant carriers: 0

GenotypeQuality
all individuals: 41492
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 9035
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2128
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2947
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 622
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2033
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.058e1

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.573e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.31e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

DP
type: SiteQuality
SIO_000300: 1.733225e6

GenotypeDepth
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 333
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2133
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variant carriers: 0

GenotypeQuality
all individuals: 9120
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 1201
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2042
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variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2948
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 129
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
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variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41865
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
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: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
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: 8642
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.931e-1

MQ
type: SiteQuality
SIO_000300: 5.627e1

DP
type: SiteQuality
SIO_000300: 1.73966e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

QD
type: SiteQuality
SIO_000300: 1.232e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.065e0

GenotypeDepth
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 9116
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41876
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 125
bin: 2.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
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
allele num: 906
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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BaseQRankSum
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SIO_000300: -2.203e0

VQSLOD
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FS
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MQ
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InbreedingCoeff
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DP
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ClippingRankSum
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SIO_000300: -8.66e-1

MQRankSum
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SIO_000300: -1.6e-1

QD
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SIO_000300: 9.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 8644
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: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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Other
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MQRankSum
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SIO_000300: -4.4e-1

ClippingRankSum
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SIO_000300: -2.03e-1

BaseQRankSum
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QD
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InbreedingCoeff
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FS
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SIO_000300: 5.7e0

VQSLOD
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

DP
type: SiteQuality
SIO_000300: 1.742438e6

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
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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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
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SIO_000300: 1.4e0

DP
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SIO_000300: 1.742919e6

QD
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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SIO_000300: 3.2e-3

MQ
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SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.648e0

ReadPosRankSum
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SIO_000300: 1.74e0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

Latino
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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: 8648
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

Other
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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
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num of homozygotes: 0

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

African
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allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.71e-1

DP
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SIO_000300: 1.743381e6

FS
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QD
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BaseQRankSum
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MQRankSum
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SIO_000300: -9.4e-2

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.47e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 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 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
allele num: 66722
num of homozygotes: 0

East Asian
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South Asian
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allele num: 16508
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Other
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African
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 18

East Asian
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allele count: 18
allele frequency: 2.082369273484498e-3
allele num: 8644
num of homozygotes: 0

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

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

African
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European (Non-Finnish)
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Other
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South Asian
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MQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 2

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

European (Finnish)
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allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

South Asian
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allele num: 16504
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
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African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
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SIO_000300: -3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 1.743623e6

QD
type: SiteQuality
SIO_000300: 1.312e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.89e-1

FS
type: SiteQuality
SIO_000300: 2.445e0

GenotypeDepth
all individuals: 52
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.401e0

DP
type: SiteQuality
SIO_000300: 1.743158e6

MQRankSum
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SIO_000300: 5.2e-2

InbreedingCoeff
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SIO_000300: -2.0e-4

QD
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SIO_000300: 1.054e1

BaseQRankSum
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SIO_000300: -3.322e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: -1.129e0

DP
type: SiteQuality
SIO_000300: 1.743174e6

VQSLOD
type: SiteQuality
SIO_000300: -5.668e-1

FS
type: SiteQuality
SIO_000300: 3.933e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.661e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

QD
type: SiteQuality
SIO_000300: 1.174e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 42091
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2932
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 617
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
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: 11578
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

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: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.69e-1

DP
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SIO_000300: 1.743159e6

BaseQRankSum
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SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.23e-1

FS
type: SiteQuality
SIO_000300: 2.675e0

QD
type: SiteQuality
SIO_000300: 9.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 334
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

Other
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.0e-4

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

DP
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MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.6e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
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
allele num: 908
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

QD
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SIO_000300: 1.398e1

BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
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FS
type: SiteQuality
SIO_000300: 3.081e0

MQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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Other
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MQRankSum
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ReadPosRankSum
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QD
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FS
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VQSLOD
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MQ
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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variant carriers: 1

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

GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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FS
type: SiteQuality
SIO_000300: 4.97e-1

ReadPosRankSum
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DP
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ClippingRankSum
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MQRankSum
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.87e-1

BaseQRankSum
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SIO_000300: 2.62e0

QD
type: SiteQuality
SIO_000300: 1.434e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 462
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

Latino
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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

South Asian
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BaseQRankSum
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SIO_000300: 2.36e-1

VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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MQ
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SIO_000300: 5.939e1

FS
type: SiteQuality
SIO_000300: 5.266e0

QD
type: SiteQuality
SIO_000300: 1.011e1

DP
type: SiteQuality
SIO_000300: 1.743262e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66724
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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MQRankSum
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DP
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ReadPosRankSum
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MQ
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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SIO_000300: 2.62e-1

InbreedingCoeff
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SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.011e1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
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allele num: 16506
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Latino
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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QD
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BaseQRankSum
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DP
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.0e-4

MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

South Asian
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Latino
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Other
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European (Finnish)
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FS
type: SiteQuality
SIO_000300: 5.48e-1

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

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

African
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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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num of homozygotes: 0

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

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

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

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

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

Other
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allele num: 906
num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 0.0e0
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African
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Other
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Latino
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allele num: 11576
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East Asian
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European (Non-Finnish)
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QD
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MQ
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
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African
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allele num: 10406
num of homozygotes: 0

Latino
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East Asian
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Other
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European (Non-Finnish)
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allele frequency: 1.199004825994425e-4
allele num: 66722
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FS
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SIO_000300: 5.24e-1

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

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

Latino
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num of homozygotes: 0

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

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

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

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66644
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Latino
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European (Finnish)
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African
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Other
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South Asian
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ReadPosRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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QD
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ClippingRankSum
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DP
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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num of homozygotes: 0

East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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Other
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VQSLOD
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InbreedingCoeff
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MQ
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ClippingRankSum
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ReadPosRankSum
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DP
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FS
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

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: 5.775895263765884e-4
allele num: 10388
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

South Asian
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allele frequency: 6.088650754992694e-5
allele num: 16424
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
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SIO_000300: 2.65e0

FS
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MQRankSum
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InbreedingCoeff
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QD
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DP
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SIO_000300: 1.739375e6

ReadPosRankSum
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SIO_000300: 1.24e0

MQ
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SIO_000300: 5.961e1

BaseQRankSum
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SIO_000300: -3.223e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.71e-1

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8642
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

Latino
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allele count: 1
allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

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

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

VQSLOD
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SIO_000300: 2.65e0

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 4.6e-3

ReadPosRankSum
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SIO_000300: 1.24e0

DP
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MQRankSum
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BaseQRankSum
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SIO_000300: -3.223e0

MQ
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SIO_000300: 5.961e1

ClippingRankSum
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SIO_000300: -7.71e-1

QD
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SIO_000300: 1.309e1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10380
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

East Asian
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allele count: 5
allele frequency: 5.787037037037037e-4
allele num: 8640
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: 8.400000000000001e-2

FS
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SIO_000300: 6.046e0

MQRankSum
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InbreedingCoeff
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SIO_000300: 5.8e-3

DP
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BaseQRankSum
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MQ
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SIO_000300: 5.93e1

ReadPosRankSum
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SIO_000300: 5.56e-1

QD
type: SiteQuality
SIO_000300: 1.347e1

VQSLOD
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SIO_000300: 1.7e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2901
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004988280545706e-5
allele num: 66556
num of homozygotes: 0

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

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

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

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

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

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

InbreedingCoeff
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SIO_000300: 6.4e-3

ReadPosRankSum
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SIO_000300: 3.34e-1

MQ
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SIO_000300: 6.0e1

QD
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ClippingRankSum
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BaseQRankSum
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FS
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SIO_000300: 3.992e0

MQRankSum
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SIO_000300: 5.74e-1

VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.73582e6

GenotypeDepth
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variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.667013347200555e-5
allele num: 11538
num of homozygotes: 0

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

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

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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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

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

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

European (Non-Finnish)
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allele frequency: 1.504890895410083e-5
allele num: 66450
num of homozygotes: 0

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

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

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

South Asian
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East Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.504890895410083e-5
allele num: 66450
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ClippingRankSum
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InbreedingCoeff
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QD
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MQ
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FS
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ReadPosRankSum
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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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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