6-163984404-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984404
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984404
    reference: chr 6
allele count: 2
allele frequency: 1.864454181038501e-5
allele num: 107270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.135-48T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.635-48T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.635-48T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*345-72T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.635-48T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440991
  ensembl transcript: ENST00000537041
  gene symbol: QKI
  hgvsc: ENST00000537041.1:c.470-72T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.635-48T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.635-72T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440599
  ensembl transcript: ENST00000544823
  gene symbol: QKI
  hgvsc: ENST00000544823.1:c.470-48T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.635-48T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.635-72T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.324-48T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.256-48T>C
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12968
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

6-163984415-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984415
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984415
    reference: chr 6
allele count: 1
allele frequency: 9.289018522302934e-6
allele num: 107654
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.635-37C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.135-37C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440991
  ensembl transcript: ENST00000537041
  gene symbol: QKI
  hgvsc: ENST00000537041.1:c.470-61C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.635-37C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440599
  ensembl transcript: ENST00000544823
  gene symbol: QKI
  hgvsc: ENST00000544823.1:c.470-37C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.635-37C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.635-37C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.635-61C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.324-37C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.635-61C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*345-61C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.635-37C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.256-37C>G
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8389
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

6-163984419-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984419
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984419
    reference: chr 6
allele count: 9
allele frequency: 8.343840391604243e-5
allele num: 107864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.635-33A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.635-33A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.135-33A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440991
  ensembl transcript: ENST00000537041
  gene symbol: QKI
  hgvsc: ENST00000537041.1:c.470-57A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.324-33A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.635-57A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.635-57A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.635-33A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.256-33A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440599
  ensembl transcript: ENST00000544823
  gene symbol: QKI
  hgvsc: ENST00000544823.1:c.470-33A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.635-33A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.635-33A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*345-57A>G
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16635
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18082
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8461
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

6-163984422-CTTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984422
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984418
    reference: chr 6
allele count: 1
allele frequency: 9.254460650033316e-6
allele num: 108056
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.635-25_635-22delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.635-25_635-22delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.324-25_324-22delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.135-25_135-22delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440991
  ensembl transcript: ENST00000537041
  gene symbol: QKI
  hgvsc: ENST00000537041.1:c.470-49_470-46delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*345-49_*345-46delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440599
  ensembl transcript: ENST00000544823
  gene symbol: QKI
  hgvsc: ENST00000544823.1:c.470-25_470-22delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.635-25_635-22delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.635-25_635-22delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.635-49_635-46delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.256-25_256-22delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.635-25_635-22delTTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.635-49_635-46delTTCT
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: CTTCT
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-163984432-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984432
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984432
    reference: chr 6
allele count: 1
allele frequency: 9.200817032552491e-6
allele num: 108686
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440991
  ensembl transcript: ENST00000537041
  gene symbol: QKI
  hgvsc: ENST00000537041.1:c.470-44A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440599
  ensembl transcript: ENST00000544823
  gene symbol: QKI
  hgvsc: ENST00000544823.1:c.470-20A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.635-20A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.635-44A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.635-20A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.324-20A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.635-20A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.135-20A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.635-44A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*345-44A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.635-20A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.256-20A>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.635-20A>C
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-163984448-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984448
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984448
    reference: chr 6
allele count: 1
allele frequency: 8.993938085730218e-6
allele num: 111186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.635-28G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.635-4G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.256-4G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.135-4G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.635-4G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440991
  ensembl transcript: ENST00000537041
  gene symbol: QKI
  hgvsc: ENST00000537041.1:c.470-28G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.635-4G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.635-28G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.635-4G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*345-28G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.324-4G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440599
  ensembl transcript: ENST00000544823
  gene symbol: QKI
  hgvsc: ENST00000544823.1:c.470-4G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.635-4G>A
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.635-4G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

6-163984483-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984483
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984483
    reference: chr 6
allele count: 2
allele frequency: 1.689075062495777e-5
allele num: 118408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440599
  ensembl transcript: ENST00000544823
  gene symbol: QKI
  hgvsc: ENST00000544823.1:c.501C>G
  hgvsp: ENST00000544823.1:c.501C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.666C>G
  hgvsp: ENST00000361758.4:c.666C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.666C>G
  hgvsp: ENST00000392127.2:c.666C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440991
  ensembl transcript: ENST00000537041
  gene symbol: QKI
  hgvsc: ENST00000537041.1:c.477C>G
  hgvsp: ENST00000537041.1:c.477C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.642C>G
  hgvsp: ENST00000424802.3:c.642C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.355C>G
  hgvsp: ENST00000537883.1:c.355C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*352C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.166C>G
  hgvsp: ENST00000544361.1:c.166C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.666C>G
  hgvsp: ENST00000361752.3:c.666C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.642C>G
  hgvsp: ENST00000361195.2:c.642C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.287C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.666C>G
  hgvsp: ENST00000275262.7:c.666C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.666C>G
  hgvsp: ENST00000453779.2:c.666C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20929
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala222Ala
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: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

6-163984490-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984490
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984490
    reference: chr 6
allele count: 1
allele frequency: 8.373806732540612e-6
allele num: 119420
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.362G>C
  hgvsp: ENSP00000441773.1:p.Ala122Pro
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.649G>C
  hgvsp: ENSP00000354867.2:p.Ala217Pro
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.673G>C
  hgvsp: ENSP00000408775.2:p.Ala225Pro
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.673G>C
  hgvsp: ENSP00000354951.4:p.Ala225Pro
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.673G>C
  hgvsp: ENSP00000355094.3:p.Ala225Pro
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.673G>C
  hgvsp: ENSP00000275262.7:p.Ala225Pro
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.673G>C
  hgvsp: ENSP00000375973.2:p.Ala225Pro
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.649G>C
  hgvsp: ENSP00000408382.3:p.Ala217Pro
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000440599
  ensembl transcript: ENST00000544823
  gene symbol: QKI
  hgvsc: ENST00000544823.1:c.508G>C
  hgvsp: ENSP00000440599.1:p.Ala170Pro
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.294G>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.173G>C
  hgvsp: ENSP00000442848.1:p.Ala59Pro
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*359G>C
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala225Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

6-163984498-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984498
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984498
    reference: chr 6
allele count: 34
allele frequency: 2.830502830502831e-4
allele num: 120120
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.681G>A
  hgvsp: ENST00000361752.3:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.681G>A
  hgvsp: ENST00000361758.4:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.302G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.681G>A
  hgvsp: ENST00000392127.2:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.181G>A
  hgvsp: ENST00000544361.1:c.181G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*367G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.681G>A
  hgvsp: ENST00000275262.7:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.657G>A
  hgvsp: ENST00000361195.2:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.657G>A
  hgvsp: ENST00000424802.3:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.370G>A
  hgvsp: ENST00000537883.1:c.370G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.681G>A
  hgvsp: ENST00000453779.2:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21471
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21434
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg227Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

6-163984506-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984506
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984506
    reference: chr 6
allele count: 2
allele frequency: 1.659310390601666e-5
allele num: 120532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.310C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.378C>G
  hgvsp: ENSP00000441773.1:p.Thr127Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.189C>G
  hgvsp: ENSP00000442848.1:p.Thr64Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.689C>G
  hgvsp: ENSP00000354951.4:p.Thr230Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.689C>G
  hgvsp: ENSP00000408775.2:p.Thr230Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.665C>G
  hgvsp: ENSP00000408382.3:p.Thr222Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.665C>G
  hgvsp: ENSP00000354867.2:p.Thr222Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.689C>G
  hgvsp: ENSP00000355094.3:p.Thr230Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.689C>G
  hgvsp: ENSP00000275262.7:p.Thr230Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*375C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.689C>G
  hgvsp: ENSP00000375973.2:p.Thr230Ser
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr230Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-163984506-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984506
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984506
    reference: chr 6
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.689C>T
  hgvsp: ENSP00000355094.3:p.Thr230Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.689C>T
  hgvsp: ENSP00000354951.4:p.Thr230Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.378C>T
  hgvsp: ENSP00000441773.1:p.Thr127Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.689C>T
  hgvsp: ENSP00000408775.2:p.Thr230Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.689C>T
  hgvsp: ENSP00000275262.7:p.Thr230Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.665C>T
  hgvsp: ENSP00000408382.3:p.Thr222Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.189C>T
  hgvsp: ENSP00000442848.1:p.Thr64Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.310C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.665C>T
  hgvsp: ENSP00000354867.2:p.Thr222Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.689C>T
  hgvsp: ENSP00000375973.2:p.Thr230Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*375C>T
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9217
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr230Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

6-163984511-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984511
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984511
    reference: chr 6
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.670C>T
  hgvsp: ENSP00000354867.2:p.Pro224Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.694C>T
  hgvsp: ENSP00000354951.4:p.Pro232Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.694C>T
  hgvsp: ENSP00000408775.2:p.Pro232Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.694C>T
  hgvsp: ENSP00000355094.3:p.Pro232Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.694C>T
  hgvsp: ENSP00000275262.7:p.Pro232Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*380C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.694C>T
  hgvsp: ENSP00000375973.2:p.Pro232Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.670C>T
  hgvsp: ENSP00000408382.3:p.Pro224Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.383C>T
  hgvsp: ENSP00000441773.1:p.Pro129Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.194C>T
  hgvsp: ENSP00000442848.1:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.315C>T
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro232Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP

6-163984515-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984515
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984515
    reference: chr 6
allele count: 1
allele frequency: 8.276501357346223e-6
allele num: 120824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.674C>T
  hgvsp: ENSP00000354867.2:p.Ala225Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*384C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.387C>T
  hgvsp: ENSP00000441773.1:p.Ala130Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.698C>T
  hgvsp: ENSP00000354951.4:p.Ala233Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.698C>T
  hgvsp: ENSP00000408775.2:p.Ala233Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.698C>T
  hgvsp: ENSP00000275262.7:p.Ala233Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.698C>T
  hgvsp: ENSP00000355094.3:p.Ala233Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.319C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.698C>T
  hgvsp: ENSP00000375973.2:p.Ala233Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.198C>T
  hgvsp: ENSP00000442848.1:p.Ala67Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.674C>T
  hgvsp: ENSP00000408382.3:p.Ala225Val
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala233Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

6-163984516-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984516
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984516
    reference: chr 6
allele count: 10
allele frequency: 8.270477702792113e-5
allele num: 120912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.388G>A
  hgvsp: ENST00000537883.1:c.388G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.699G>A
  hgvsp: ENST00000361752.3:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.199G>A
  hgvsp: ENST00000544361.1:c.199G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.699G>A
  hgvsp: ENST00000275262.7:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.699G>A
  hgvsp: ENST00000361758.4:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.699G>A
  hgvsp: ENST00000453779.2:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.675G>A
  hgvsp: ENST00000361195.2:c.675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.675G>A
  hgvsp: ENST00000424802.3:c.675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*385G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.699G>A
  hgvsp: ENST00000392127.2:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.320G>A
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9286
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala233Ala
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum

6-163984517-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984517
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984517
    reference: chr 6
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.700C>T
  hgvsp: ENSP00000354951.4:p.Pro234Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.700C>T
  hgvsp: ENSP00000355094.3:p.Pro234Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.676C>T
  hgvsp: ENSP00000354867.2:p.Pro226Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.200C>T
  hgvsp: ENSP00000442848.1:p.Pro68Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.389C>T
  hgvsp: ENSP00000441773.1:p.Pro131Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*386C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.700C>T
  hgvsp: ENSP00000408775.2:p.Pro234Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.676C>T
  hgvsp: ENSP00000408382.3:p.Pro226Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.700C>T
  hgvsp: ENSP00000275262.7:p.Pro234Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.321C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.700C>T
  hgvsp: ENSP00000375973.2:p.Pro234Ser
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro234Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

6-163984519-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984519
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984519
    reference: chr 6
allele count: 2
allele frequency: 1.652755970580944e-5
allele num: 121010
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.678G>C
  hgvsp: ENST00000424802.3:c.678G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.391G>C
  hgvsp: ENST00000537883.1:c.391G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.678G>C
  hgvsp: ENST00000361195.2:c.678G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.702G>C
  hgvsp: ENST00000361752.3:c.702G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.702G>C
  hgvsp: ENST00000453779.2:c.702G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.323G>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.702G>C
  hgvsp: ENST00000275262.7:c.702G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.202G>C
  hgvsp: ENST00000544361.1:c.202G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*388G>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.702G>C
  hgvsp: ENST00000392127.2:c.702G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.702G>C
  hgvsp: ENST00000361758.4:c.702G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro234Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum

6-163984528-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984528
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984528
    reference: chr 6
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.711A>G
  hgvsp: ENST00000453779.2:c.711A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.711A>G
  hgvsp: ENST00000361758.4:c.711A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.211A>G
  hgvsp: ENST00000544361.1:c.211A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.711A>G
  hgvsp: ENST00000361752.3:c.711A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.400A>G
  hgvsp: ENST00000537883.1:c.400A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.711A>G
  hgvsp: ENST00000392127.2:c.711A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.687A>G
  hgvsp: ENST00000424802.3:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.687A>G
  hgvsp: ENST00000361195.2:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*397A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.711A>G
  hgvsp: ENST00000275262.7:c.711A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.332A>G
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro237Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

6-163984535-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984535
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984535
    reference: chr 6
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.718G>T
  hgvsp: ENSP00000375973.2:p.Ala240Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.339G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*404G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.718G>T
  hgvsp: ENSP00000354951.4:p.Ala240Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.718G>T
  hgvsp: ENSP00000355094.3:p.Ala240Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.694G>T
  hgvsp: ENSP00000354867.2:p.Ala232Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.218G>T
  hgvsp: ENSP00000442848.1:p.Ala74Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.718G>T
  hgvsp: ENSP00000275262.7:p.Ala240Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.694G>T
  hgvsp: ENSP00000408382.3:p.Ala232Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.407G>T
  hgvsp: ENSP00000441773.1:p.Ala137Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.718G>T
  hgvsp: ENSP00000408775.2:p.Ala240Ser
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21193
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala240Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

6-163984537-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984537
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984537
    reference: chr 6
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.720C>T
  hgvsp: ENST00000392127.2:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.720C>T
  hgvsp: ENST00000361752.3:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.696C>T
  hgvsp: ENST00000361195.2:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.696C>T
  hgvsp: ENST00000424802.3:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.720C>T
  hgvsp: ENST00000361758.4:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.220C>T
  hgvsp: ENST00000544361.1:c.220C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*406C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.720C>T
  hgvsp: ENST00000275262.7:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.720C>T
  hgvsp: ENST00000453779.2:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.341C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.409C>T
  hgvsp: ENST00000537883.1:c.409C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala240Ala
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

6-163984552-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984552
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984552
    reference: chr 6
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.735G>A
  hgvsp: ENST00000392127.2:c.735G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.356G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.711G>A
  hgvsp: ENST00000361195.2:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.235G>A
  hgvsp: ENST00000544361.1:c.235G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.735G>A
  hgvsp: ENST00000361752.3:c.735G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.424G>A
  hgvsp: ENST00000537883.1:c.424G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.735G>A
  hgvsp: ENST00000453779.2:c.735G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.735G>A
  hgvsp: ENST00000275262.7:c.735G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.735G>A
  hgvsp: ENST00000361758.4:c.735G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.711G>A
  hgvsp: ENST00000424802.3:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*421G>A
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr245Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

6-163984552-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984552
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984552
    reference: chr 6
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.735G>T
  hgvsp: ENST00000275262.7:c.735G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.735G>T
  hgvsp: ENST00000361752.3:c.735G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.735G>T
  hgvsp: ENST00000361758.4:c.735G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.356G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.711G>T
  hgvsp: ENST00000361195.2:c.711G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.711G>T
  hgvsp: ENST00000424802.3:c.711G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.735G>T
  hgvsp: ENST00000392127.2:c.735G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.235G>T
  hgvsp: ENST00000544361.1:c.235G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.735G>T
  hgvsp: ENST00000453779.2:c.735G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*421G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.424G>T
  hgvsp: ENST00000537883.1:c.424G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr245Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

6-163984555-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984555
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984555
    reference: chr 6
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.738A>G
  hgvsp: ENST00000361758.4:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.738A>G
  hgvsp: ENST00000361752.3:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.738A>G
  hgvsp: ENST00000453779.2:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.714A>G
  hgvsp: ENST00000424802.3:c.714A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.238A>G
  hgvsp: ENST00000544361.1:c.238A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*424A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.714A>G
  hgvsp: ENST00000361195.2:c.714A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.427A>G
  hgvsp: ENST00000537883.1:c.427A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.738A>G
  hgvsp: ENST00000275262.7:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.359A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.738A>G
  hgvsp: ENST00000392127.2:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro246Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

6-163984567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984567
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984567
    reference: chr 6
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.750C>T
  hgvsp: ENST00000275262.7:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*436C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.750C>T
  hgvsp: ENST00000361758.4:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.726C>T
  hgvsp: ENST00000361195.2:c.726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.750C>T
  hgvsp: ENST00000453779.2:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.750C>T
  hgvsp: ENST00000392127.2:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.750C>T
  hgvsp: ENST00000361752.3:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.250C>T
  hgvsp: ENST00000544361.1:c.250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.726C>T
  hgvsp: ENST00000424802.3:c.726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.439C>T
  hgvsp: ENST00000537883.1:c.439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.371C>T
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr250Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

6-163984594-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984594
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984594
    reference: chr 6
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.777G>C
  hgvsp: ENSP00000408775.2:p.Gln259His
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.777G>C
  hgvsp: ENSP00000275262.7:p.Gln259His
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.753G>C
  hgvsp: ENSP00000354867.2:p.Gln251His
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.466G>C
  hgvsp: ENSP00000441773.1:p.Gln156His
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.777G>C
  hgvsp: ENSP00000354951.4:p.Gln259His
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.277G>C
  hgvsp: ENSP00000442848.1:p.Gln93His
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.777G>C
  hgvsp: ENSP00000375973.2:p.Gln259His
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.753G>C
  hgvsp: ENSP00000408382.3:p.Gln251His
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.777G>C
  hgvsp: ENSP00000355094.3:p.Gln259His
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.398G>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*463G>C
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln259His
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-163984597-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984597
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984597
    reference: chr 6
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.280C>A
  hgvsp: ENST00000544361.1:c.280C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.780C>A
  hgvsp: ENST00000275262.7:c.780C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.469C>A
  hgvsp: ENST00000537883.1:c.469C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.780C>A
  hgvsp: ENST00000453779.2:c.780C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.780C>A
  hgvsp: ENST00000361758.4:c.780C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.756C>A
  hgvsp: ENST00000424802.3:c.756C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*466C>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.756C>A
  hgvsp: ENST00000361195.2:c.756C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.780C>A
  hgvsp: ENST00000361752.3:c.780C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.780C>A
  hgvsp: ENST00000392127.2:c.780C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.401C>A
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22766
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr260Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

6-163984597-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984597
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984597
    reference: chr 6
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.469C>T
  hgvsp: ENST00000537883.1:c.469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*466C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.780C>T
  hgvsp: ENST00000275262.7:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.780C>T
  hgvsp: ENST00000392127.2:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.756C>T
  hgvsp: ENST00000361195.2:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.756C>T
  hgvsp: ENST00000424802.3:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.780C>T
  hgvsp: ENST00000361752.3:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.401C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.280C>T
  hgvsp: ENST00000544361.1:c.280C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.780C>T
  hgvsp: ENST00000361758.4:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.780C>T
  hgvsp: ENST00000453779.2:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr260Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

6-163984598-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984598
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984598
    reference: chr 6
allele count: 3
allele frequency: 2.472065658063878e-5
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.781G>A
  hgvsp: ENSP00000355094.3:p.Ala261Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.781G>A
  hgvsp: ENSP00000375973.2:p.Ala261Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.781G>A
  hgvsp: ENSP00000275262.7:p.Ala261Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.757G>A
  hgvsp: ENSP00000408382.3:p.Ala253Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.781G>A
  hgvsp: ENSP00000354951.4:p.Ala261Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.781G>A
  hgvsp: ENSP00000408775.2:p.Ala261Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.757G>A
  hgvsp: ENSP00000354867.2:p.Ala253Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.281G>A
  hgvsp: ENSP00000442848.1:p.Ala95Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.402G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.470G>A
  hgvsp: ENSP00000441773.1:p.Ala158Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*467G>A
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala261Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

6-163984600-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984600
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984600
    reference: chr 6
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.759T>C
  hgvsp: ENST00000361195.2:c.759T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.283T>C
  hgvsp: ENST00000544361.1:c.283T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.783T>C
  hgvsp: ENST00000453779.2:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.472T>C
  hgvsp: ENST00000537883.1:c.472T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.783T>C
  hgvsp: ENST00000392127.2:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.783T>C
  hgvsp: ENST00000275262.7:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.404T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.759T>C
  hgvsp: ENST00000424802.3:c.759T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.783T>C
  hgvsp: ENST00000361758.4:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.783T>C
  hgvsp: ENST00000361752.3:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*469T>C
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala261Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD

6-163984609-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984609
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984609
    reference: chr 6
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.768A>G
  hgvsp: ENST00000361195.2:c.768A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.481A>G
  hgvsp: ENST00000537883.1:c.481A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*478A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.792A>G
  hgvsp: ENST00000453779.2:c.792A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.792A>G
  hgvsp: ENST00000361752.3:c.792A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.292A>G
  hgvsp: ENST00000544361.1:c.292A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.413A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.792A>G
  hgvsp: ENST00000361758.4:c.792A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.792A>G
  hgvsp: ENST00000275262.7:c.792A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.768A>G
  hgvsp: ENST00000424802.3:c.768A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.792A>G
  hgvsp: ENST00000392127.2:c.792A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro264Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

6-163984611-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984611
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984611
    reference: chr 6
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.415A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.794A>G
  hgvsp: ENSP00000275262.7:p.Asn265Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.794A>G
  hgvsp: ENSP00000354951.4:p.Asn265Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.794A>G
  hgvsp: ENSP00000408775.2:p.Asn265Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.483A>G
  hgvsp: ENSP00000441773.1:p.Asn162Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*480A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.794A>G
  hgvsp: ENSP00000355094.3:p.Asn265Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.770A>G
  hgvsp: ENSP00000354867.2:p.Asn257Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.294A>G
  hgvsp: ENSP00000442848.1:p.Asn99Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.770A>G
  hgvsp: ENSP00000408382.3:p.Asn257Ser
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.794A>G
  hgvsp: ENSP00000375973.2:p.Asn265Ser
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn265Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-163984612-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984612
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984612
    reference: chr 6
allele count: 8
allele frequency: 6.592175088170342e-5
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.795C>T
  hgvsp: ENST00000392127.2:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.795C>T
  hgvsp: ENST00000361752.3:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.484C>T
  hgvsp: ENST00000537883.1:c.484C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*481C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.771C>T
  hgvsp: ENST00000361195.2:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.771C>T
  hgvsp: ENST00000424802.3:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.795C>T
  hgvsp: ENST00000275262.7:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.795C>T
  hgvsp: ENST00000453779.2:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.795C>T
  hgvsp: ENST00000361758.4:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.416C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.295C>T
  hgvsp: ENST00000544361.1:c.295C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22781
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 21128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn265Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

6-163984623-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984623
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984623
    reference: chr 6
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.782A>T
  hgvsp: ENSP00000408382.3:p.His261Leu
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.806A>T
  hgvsp: ENSP00000408775.2:p.His269Leu
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.806A>T
  hgvsp: ENSP00000355094.3:p.His269Leu
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*492A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.806A>T
  hgvsp: ENSP00000354951.4:p.His269Leu
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.782A>T
  hgvsp: ENSP00000354867.2:p.His261Leu
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.427A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.306A>T
  hgvsp: ENSP00000442848.1:p.His103Leu
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.806A>T
  hgvsp: ENSP00000275262.7:p.His269Leu
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.806A>T
  hgvsp: ENSP00000375973.2:p.His269Leu
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.495A>T
  hgvsp: ENSP00000441773.1:p.His166Leu
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His269Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS

6-163984628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984628
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984628
    reference: chr 6
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.811A>G
  hgvsp: ENSP00000354951.4:p.Thr271Ala
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.311A>G
  hgvsp: ENSP00000442848.1:p.Thr105Ala
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.432A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.811A>G
  hgvsp: ENSP00000408775.2:p.Thr271Ala
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.811A>G
  hgvsp: ENSP00000355094.3:p.Thr271Ala
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.811A>G
  hgvsp: ENSP00000375973.2:p.Thr271Ala
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*497A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.787A>G
  hgvsp: ENSP00000354867.2:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.811A>G
  hgvsp: ENSP00000275262.7:p.Thr271Ala
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.787A>G
  hgvsp: ENSP00000408382.3:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.500A>G
  hgvsp: ENSP00000441773.1:p.Thr168Ala
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr271Ala
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

6-163984637-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984637
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984637
    reference: chr 6
allele count: 3
allele frequency: 2.471984179301253e-5
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.820A>G
  hgvsp: ENSP00000354951.4:p.Ile274Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.820A>G
  hgvsp: ENSP00000408775.2:p.Ile274Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.820A>G
  hgvsp: ENSP00000275262.7:p.Ile274Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.796A>G
  hgvsp: ENSP00000408382.3:p.Ile266Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*506A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.820A>G
  hgvsp: ENSP00000375973.2:p.Ile274Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.796A>G
  hgvsp: ENSP00000354867.2:p.Ile266Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.509A>G
  hgvsp: ENSP00000441773.1:p.Ile171Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.820A>G
  hgvsp: ENSP00000355094.3:p.Ile274Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.441A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.320A>G
  hgvsp: ENSP00000442848.1:p.Ile108Val
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile274Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

6-163984654-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984654
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984654
    reference: chr 6
allele count: 14
allele frequency: 1.153592617007251e-4
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.837C>T
  hgvsp: ENST00000361758.4:c.837C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.337C>T
  hgvsp: ENST00000544361.1:c.337C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.813C>T
  hgvsp: ENST00000424802.3:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.813C>T
  hgvsp: ENST00000361195.2:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.526C>T
  hgvsp: ENST00000537883.1:c.526C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.837C>T
  hgvsp: ENST00000361752.3:c.837C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.837C>T
  hgvsp: ENST00000453779.2:c.837C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.837C>T
  hgvsp: ENST00000275262.7:c.837C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*523C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.458C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.837C>T
  hgvsp: ENST00000392127.2:c.837C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro279Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

6-163984660-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984660
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984660
    reference: chr 6
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.464T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.343T>G
  hgvsp: ENST00000544361.1:c.343T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.819T>G
  hgvsp: ENST00000424802.3:c.819T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.532T>G
  hgvsp: ENST00000537883.1:c.532T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.843T>G
  hgvsp: ENST00000392127.2:c.843T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*529T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.819T>G
  hgvsp: ENST00000361195.2:c.819T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.843T>G
  hgvsp: ENST00000275262.7:c.843T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.843T>G
  hgvsp: ENST00000361752.3:c.843T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.843T>G
  hgvsp: ENST00000453779.2:c.843T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.843T>G
  hgvsp: ENST00000361758.4:c.843T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala281Ala
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-163984669-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984669
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984669
    reference: chr 6
allele count: 13
allele frequency: 1.071175491504754e-4
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.852C>T
  hgvsp: ENST00000275262.7:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.541C>T
  hgvsp: ENST00000537883.1:c.541C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.828C>T
  hgvsp: ENST00000361195.2:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.352C>T
  hgvsp: ENST00000544361.1:c.352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.828C>T
  hgvsp: ENST00000424802.3:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.852C>T
  hgvsp: ENST00000361752.3:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*538C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.852C>T
  hgvsp: ENST00000361758.4:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.852C>T
  hgvsp: ENST00000392127.2:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.852C>T
  hgvsp: ENST00000453779.2:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.473C>T
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile284Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

6-163984697-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984697
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984697
    reference: chr 6
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.856T>C
  hgvsp: ENST00000424802.3:c.856T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.880T>C
  hgvsp: ENST00000361752.3:c.880T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.880T>C
  hgvsp: ENST00000453779.2:c.880T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*566T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.880T>C
  hgvsp: ENST00000361758.4:c.880T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.880T>C
  hgvsp: ENST00000275262.7:c.880T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.880T>C
  hgvsp: ENST00000392127.2:c.880T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.380T>C
  hgvsp: ENST00000544361.1:c.380T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.501T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.856T>C
  hgvsp: ENST00000361195.2:c.856T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.569T>C
  hgvsp: ENST00000537883.1:c.569T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu294Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum

6-163984700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984700
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984700
    reference: chr 6
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.572G>A
  hgvsp: ENSP00000441773.1:p.Ala192Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.883G>A
  hgvsp: ENSP00000375973.2:p.Ala295Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.883G>A
  hgvsp: ENSP00000355094.3:p.Ala295Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.883G>A
  hgvsp: ENSP00000354951.4:p.Ala295Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.383G>A
  hgvsp: ENSP00000442848.1:p.Ala129Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.859G>A
  hgvsp: ENSP00000408382.3:p.Ala287Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*569G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.859G>A
  hgvsp: ENSP00000354867.2:p.Ala287Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.883G>A
  hgvsp: ENSP00000408775.2:p.Ala295Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.883G>A
  hgvsp: ENSP00000275262.7:p.Ala295Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.504G>A
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala295Thr
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

6-163984711-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984711
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984711
    reference: chr 6
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*580A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.894A>T
  hgvsp: ENST00000275262.7:c.894A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.894A>T
  hgvsp: ENST00000453779.2:c.894A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.870A>T
  hgvsp: ENST00000361195.2:c.870A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.894A>T
  hgvsp: ENST00000361752.3:c.894A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.870A>T
  hgvsp: ENST00000424802.3:c.870A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.515A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.894A>T
  hgvsp: ENST00000361758.4:c.894A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.394A>T
  hgvsp: ENST00000544361.1:c.394A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.894A>T
  hgvsp: ENST00000392127.2:c.894A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.583A>T
  hgvsp: ENST00000537883.1:c.583A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr298Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-163984730-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984730
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984730
    reference: chr 6
allele count: 3
allele frequency: 2.483238142537869e-5
allele num: 120810
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.889A>G
  hgvsp: ENSP00000408382.3:p.Ile297Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.913A>G
  hgvsp: ENSP00000408775.2:p.Ile305Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*599A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.913A>G
  hgvsp: ENSP00000354951.4:p.Ile305Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.413A>G
  hgvsp: ENSP00000442848.1:p.Ile139Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.602A>G
  hgvsp: ENSP00000441773.1:p.Ile202Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.913A>G
  hgvsp: ENSP00000355094.3:p.Ile305Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.913A>G
  hgvsp: ENSP00000275262.7:p.Ile305Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.889A>G
  hgvsp: ENSP00000354867.2:p.Ile297Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.534A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.913A>G
  hgvsp: ENSP00000375973.2:p.Ile305Val
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile305Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-163984731-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984731
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984731
    reference: chr 6
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.914T>C
  hgvsp: ENSP00000355094.3:p.Ile305Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.890T>C
  hgvsp: ENSP00000408382.3:p.Ile297Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.914T>C
  hgvsp: ENSP00000275262.7:p.Ile305Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.914T>C
  hgvsp: ENSP00000375973.2:p.Ile305Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.890T>C
  hgvsp: ENSP00000354867.2:p.Ile297Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.914T>C
  hgvsp: ENSP00000354951.4:p.Ile305Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.603T>C
  hgvsp: ENSP00000441773.1:p.Ile202Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.414T>C
  hgvsp: ENSP00000442848.1:p.Ile139Thr
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*600T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.535T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.914T>C
  hgvsp: ENSP00000408775.2:p.Ile305Thr
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile305Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP

6-163984740-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984740
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984740
    reference: chr 6
allele count: 1
allele frequency: 8.318913882603488e-6
allele num: 120208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.423G>T
  hgvsp: ENSP00000442848.1:p.Ser142Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*609G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.899G>T
  hgvsp: ENSP00000408382.3:p.Ser300Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.923G>T
  hgvsp: ENSP00000354951.4:p.Ser308Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.923G>T
  hgvsp: ENSP00000275262.7:p.Ser308Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.923G>T
  hgvsp: ENSP00000375973.2:p.Ser308Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.544G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.923G>T
  hgvsp: ENSP00000355094.3:p.Ser308Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.899G>T
  hgvsp: ENSP00000354867.2:p.Ser300Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.612G>T
  hgvsp: ENSP00000441773.1:p.Ser205Ile
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.923G>T
  hgvsp: ENSP00000408775.2:p.Ser308Ile
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser308Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS

6-163984744-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984744
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984744
    reference: chr 6
allele count: 1
allele frequency: 8.34153584357952e-6
allele num: 119882
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.548T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.927T>C
  hgvsp: ENST00000361752.3:c.927T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.927T>C
  hgvsp: ENST00000361758.4:c.927T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.903T>C
  hgvsp: ENST00000361195.2:c.903T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*613T>C
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.903T>C
  hgvsp: ENST00000424802.3:c.903T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.927T>C
  hgvsp: ENST00000392127.2:c.927T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.427T>C
  hgvsp: ENST00000544361.1:c.427T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.616T>C
  hgvsp: ENST00000537883.1:c.616T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.927T>C
  hgvsp: ENST00000453779.2:c.927T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.927T>C
  hgvsp: ENST00000275262.7:c.927T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19963
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly309Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-163984747-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984747
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984747
    reference: chr 6
allele count: 5
allele frequency: 4.181091432107437e-5
allele num: 119586
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.906A>G
  hgvsp: ENST00000361195.2:c.906A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.906A>G
  hgvsp: ENST00000424802.3:c.906A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.930A>G
  hgvsp: ENST00000361758.4:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.930A>G
  hgvsp: ENST00000453779.2:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.619A>G
  hgvsp: ENST00000537883.1:c.619A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.930A>G
  hgvsp: ENST00000392127.2:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.930A>G
  hgvsp: ENST00000275262.7:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.430A>G
  hgvsp: ENST00000544361.1:c.430A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.930A>G
  hgvsp: ENST00000361752.3:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*616A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.551A>G
  variant of: http://identifiers.org/hgnc/21100
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val310Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

6-163984756-GTTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984756
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984753
    reference: chr 6
allele count: 6
allele frequency: 5.055100596501871e-5
allele num: 118692
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+10_934+12delTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+10_555+12delTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+10_934+12delTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+10_934+12delTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+10_910+12delTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+10_623+12delTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.944_946delTCT
  hgvsp: ENSP00000375973.2:p.Phe315del
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+10_910+12delTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+10_434+12delTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+10_934+12delTCT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+10_*620+12delTCT
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Phe315del
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: GTTC
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

6-163984766-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984766
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984766
    reference: chr 6
allele count: 1
allele frequency: 8.553441905022582e-6
allele num: 116912
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+15C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+15C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+15C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+15C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+15C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+15C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+15C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+15C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+15C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.949C>G
  hgvsp: ENSP00000375973.2:p.Pro317Ala
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+15C>G
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro317Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS

6-163984768-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984768
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984768
    reference: chr 6
allele count: 17
allele frequency: 1.457201145188665e-4
allele num: 116662
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+17A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.951A>G
  hgvsp: ENST00000392127.2:c.951A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+17A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+17A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+17A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+17A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+17A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+17A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+17A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+17A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+17A>G
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21246
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro317Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

6-163984773-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984773
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984773
    reference: chr 6
allele count: 1
allele frequency: 8.640353908896108e-6
allele num: 115736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+22G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+22G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+22G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.956G>T
  hgvsp: ENSP00000375973.2:p.Gly319Val
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+22G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+22G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+22G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+22G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+22G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+22G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+22G>T
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3296
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly319Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

6-163984779-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984779
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984779
    reference: chr 6
allele count: 3
allele frequency: 2.61798380340687e-5
allele num: 114592
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+28A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+28A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+28A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+28A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+28A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+28A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+28A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*2A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+28A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+28A>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+28A>G
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9061
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

6-163984782-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984782
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984782
    reference: chr 6
allele count: 1
allele frequency: 8.80839968994433e-6
allele num: 113528
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+31A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+31A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*5A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+31A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+31A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+31A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+31A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+31A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+31A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+31A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+31A>T
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4647
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

6-163984785-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984785
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984785
    reference: chr 6
allele count: 1
allele frequency: 8.85065406333528e-6
allele num: 112986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+34C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+34C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+34C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+34C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+34C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*8C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+34C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+34C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+34C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+34C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+34C>T
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

6-163984803-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984803
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984803
    reference: chr 6
allele count: 1
allele frequency: 9.104317267248129e-6
allele num: 109838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+52G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+52G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+52G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*26G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+52G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+52G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+52G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+52G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+52G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+52G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+52G>A
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

6-163984806-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984806
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984806
    reference: chr 6
allele count: 1
allele frequency: 9.148628620569777e-6
allele num: 109306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+55C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+55C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+55C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+55C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+55C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+55C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+55C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+55C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+55C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*29C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+55C>T
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

6-163984821-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984821
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984822
    reference: chr 6
allele count: 1
allele frequency: 9.263033087554189e-6
allele num: 107956
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+71dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+71dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+71dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*45dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+71dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+71dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+71dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+71dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+71dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+71dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+71dupT
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13287
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4319
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

6-163984824-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984824
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984824
    reference: chr 6
allele count: 7
allele frequency: 6.503762891387159e-5
allele num: 107630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+73A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+73A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*47A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+73A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+73A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+73A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+73A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+73A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+73A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+73A>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+73A>T
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8087
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13319
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14440
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2429
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

6-163984827-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163984827
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163984827
    reference: chr 6
allele count: 1
allele frequency: 9.359264736162327e-6
allele num: 106846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+76T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+76T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.555+76T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+76T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+76T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.910+76T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*50T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+76T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+76T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+76T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.934+76T>G
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

6-163985655-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163985655
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163985655
    reference: chr 6
allele count: 13535
allele frequency: 1.116233423500693e-1
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+904G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+904G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+904G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.556-44G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*878G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+904G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.935-44G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+904G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+904G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.911-44G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+904G>A
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 6.75e1
  variant carriers: 1069
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 4.25e1
  variant carriers: 1014
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 7.25e1
  variant carriers: 922
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 2.75e1
  variant carriers: 287
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 2.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 9.25e1
  variant carriers: 263
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 3.25e1
  variant carriers: 504
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 5.25e1
  variant carriers: 1226
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6644
  bin: 4.75e1
  variant carriers: 1153
genotype depth: GenotypeDepth
  all individuals: 6109
  bin: 5.75e1
  variant carriers: 1255
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 9.75e1
  variant carriers: 1040
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 3.75e1
  variant carriers: 870
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 7.75e1
  variant carriers: 711
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 8.25e1
  variant carriers: 514
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 6.25e1
  variant carriers: 1155
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 8.75e1
  variant carriers: 389
genotype quality: GenotypeQuality
  all individuals: 49769
  bin: 9.75e1
  variant carriers: 12492
num of homozygotes: 963
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

6-163985657-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163985657
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163985657
    reference: chr 6
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+906G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.556-42G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+906G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+906G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.935-42G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+906G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*880G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+906G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+906G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+906G>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.911-42G>T
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6734
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1199
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

6-163985660-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163985660
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163985660
    reference: chr 6
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*883G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.556-39G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+909G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.935-39G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+909G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+909G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+909G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+909G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+909G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.911-39G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+909G>A
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6735
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

6-163985665-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163985665
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163985665
    reference: chr 6
allele count: 3
allele frequency: 2.472921509471289e-5
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+914C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+914C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+914C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.556-34C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+914C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*888C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+914C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.911-34C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+914C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+914C>T
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.935-34C>T
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6737
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6736
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2145
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

6-163985666-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163985666
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163985666
    reference: chr 6
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+915G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.935-33G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.911-33G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+915G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*889G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+915G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+915G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+915G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+915G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+915G>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.556-33G>A
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6739
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

6-163985677-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163985677
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163985677
    reference: chr 6
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.911-22T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+926T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+926T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*900T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.556-22T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+926T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+926T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+926T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+926T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.935-22T>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+926T>G
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6735
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-163985685-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163985685
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163985685
    reference: chr 6
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+934C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+934C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+934C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.911-14C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.935-14C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+934C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*908C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+934C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.556-14C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+934C>G
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+934C>G
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

6-163985686-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163985686
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163985687
    reference: chr 6
allele count: 1
allele frequency: 8.271298593879239e-6
allele num: 120900
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+943dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.911-5dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+943dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.556-5dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+943dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.935-5dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+943dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+943dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*917dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+943dupT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+943dupT
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6195
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6799
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

6-163985686-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163985686
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163985685
    reference: chr 6
allele count: 9
allele frequency: 7.444168734491315e-5
allele num: 120900
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+943delT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.556-5delT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+943delT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+943delT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+943delT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.911-5delT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+943delT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*917delT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+943delT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.935-5delT
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+943delT
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6799
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6195
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1819
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: CT
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

6-163985689-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163985689
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163985689
    reference: chr 6
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+938T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+938T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.935-10T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*912T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+938T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+938T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+938T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.911-10T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+938T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.556-10T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+938T>A
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6788
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP

6-163985694-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 163985694
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 163985694
    reference: chr 6
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000441773
  ensembl transcript: ENST00000537883
  gene symbol: QKI
  hgvsc: ENST00000537883.1:c.623+943T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000275262
  ensembl transcript: ENST00000275262
  gene symbol: QKI
  hgvsc: ENST00000275262.7:c.935-5T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000355094
  ensembl transcript: ENST00000361752
  gene symbol: QKI
  hgvsc: ENST00000361752.3:c.934+943T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl transcript: ENST00000540719
  gene symbol: QKI
  hgvsc: ENST00000540719.1:n.556-5T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408775
  ensembl transcript: ENST00000453779
  gene symbol: QKI
  hgvsc: ENST00000453779.2:c.934+943T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354867
  ensembl transcript: ENST00000361195
  gene symbol: QKI
  hgvsc: ENST00000361195.2:c.910+943T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000437867
  ensembl transcript: ENST00000545607
  gene symbol: QKI
  hgvsc: ENST00000545607.1:c.*620+943T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000354951
  ensembl transcript: ENST00000361758
  gene symbol: QKI
  hgvsc: ENST00000361758.4:c.934+943T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000408382
  ensembl transcript: ENST00000424802
  gene symbol: QKI
  hgvsc: ENST00000424802.3:c.911-5T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000375973
  ensembl transcript: ENST00000392127
  gene symbol: QKI
  hgvsc: ENST00000392127.2:c.*917T>A
  variant of: http://identifiers.org/hgnc/21100
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112531
  ensembl protein: ENSP00000442848
  ensembl transcript: ENST00000544361
  gene symbol: QKI
  hgvsc: ENST00000544361.1:c.434+943T>A
  variant of: http://identifiers.org/hgnc/21100
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6766
  bin: 4.75e1
  variant carriers: 0
hgvs: n.556-5T>A
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 371
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 306
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 226
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21217
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7862
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1510
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2479
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2198
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4375
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1421
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1853
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2089
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3397
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2831
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2272
bin: 8.25e1
variant carriers: 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: 8370
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.122082585278277e-4
allele num: 8912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.621165942545879e-5
allele num: 61684
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.078e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.891e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

VQSLOD
type: SiteQuality
SIO_000300: -2.152e-1

DP
type: SiteQuality
SIO_000300: 1.518385e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e0

GenotypeDepth
all individuals: 3104
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1427
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 713
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 306
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4370
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 642
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3329
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7963
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3734
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26328
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2793
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.615352308338448e-5
allele num: 61906
num of homozygotes: 0

South Asian
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: 6584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

FS
type: SiteQuality
SIO_000300: 1.556e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.167e1

VQSLOD
type: SiteQuality
SIO_000300: 5.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.04e-1

DP
type: SiteQuality
SIO_000300: 1.550626e6

GenotypeDepth
all individuals: 60
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 714
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4231
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3331
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8008
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GenotypeQuality
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GenotypeQuality
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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: 4381
bin: 9.75e1
variant carriers: 9

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8978
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 9.232663110381617e-4
allele num: 9748
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61986
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.083e0

VQSLOD
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MQRankSum
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SIO_000300: -7.9e-2

DP
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BaseQRankSum
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SIO_000300: 2.55e0

QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 1.019160211985324e-4
allele num: 9812
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62072
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8994
num of homozygotes: 0

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

DP
type: SiteQuality
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QD
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FS
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SIO_000300: 0.0e0

MQ
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VQSLOD
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InbreedingCoeff
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SIO_000300: -3.3e-3

BaseQRankSum
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SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: -4.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

ReadPosRankSum
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SIO_000300: 3.95e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.103509159126021e-4
allele num: 9062
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62342
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: 1.16e0

MQRankSum
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SIO_000300: 4.45e-1

QD
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SIO_000300: 1.535e1

DP
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InbreedingCoeff
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SIO_000300: -2.3e-3

MQ
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SIO_000300: 5.94e1

FS
type: SiteQuality
SIO_000300: 1.066e0

VQSLOD
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SIO_000300: 5.629999999999999e-1

ClippingRankSum
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SIO_000300: -4.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.57693884631154e-5
allele num: 63414
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9444
num of homozygotes: 0

Latino
type: Population
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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.421e0

BaseQRankSum
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SIO_000300: -3.818e0

ReadPosRankSum
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SIO_000300: -2.25e-1

DP
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SIO_000300: 1.614283e6

VQSLOD
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SIO_000300: 8.99e-1

MQRankSum
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SIO_000300: 9.6e-2

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-1

QD
type: SiteQuality
SIO_000300: 1.446e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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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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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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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

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

East Asian
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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

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

QD
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SIO_000300: 1.066e1

ClippingRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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SIO_000300: 5.918e1

MQRankSum
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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: 1

Other
type: Population
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allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65952
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
type: Population
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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: 11504
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: 1
allele frequency: 9.72762645914397e-5
allele num: 10280
num of homozygotes: 0

DP
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SIO_000300: 1.697855e6

FS
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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QD
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SIO_000300: 1.417e1

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: 34
allele frequency: 2.950876583926402e-3
allele num: 11522
num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 0.0e0
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: -4.47e-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
all individuals: 1167
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.015317814497648e-5
allele num: 66328
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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

MQ
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SIO_000300: 6.0e1

DP
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
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SIO_000300: 1.28e1

FS
type: SiteQuality
SIO_000300: 4.249e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

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

Other
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allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66328
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11520
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: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -5.14e-1

VQSLOD
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SIO_000300: 7.73e-1

InbreedingCoeff
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MQRankSum
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MQ
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QD
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SIO_000300: 1.28e1

ReadPosRankSum
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SIO_000300: 5.22e-1

FS
type: SiteQuality
SIO_000300: 4.249e0

DP
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SIO_000300: 1.713209e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-2

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: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506250941406838e-5
allele num: 66390
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 4.75e-1

InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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QD
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MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 1.716617e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 925
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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
all individuals: 2273
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505253334136135e-5
allele num: 66434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
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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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African
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.616e0

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 5.5e-3

DP
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SIO_000300: 1.719595e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.7e-2

MQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.414e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

GenotypeDepth
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.73550850399167e-4
allele num: 11524
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.131970260223048e-4
allele num: 8608
num of homozygotes: 0

European (Finnish)
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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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504664459825459e-5
allele num: 66460
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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DP
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QD
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SIO_000300: 1.406e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 3.209e0

MQRankSum
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SIO_000300: 3.3e-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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bin: 4.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504438092372499e-5
allele num: 66470
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
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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Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -5.096e0

VQSLOD
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SIO_000300: 9.5e-1

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.005981903988938e-5
allele num: 66534
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66728
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European (Finnish)
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Latino
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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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ReadPosRankSum
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ClippingRankSum
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QD
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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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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South Asian
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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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European (Non-Finnish)
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allele num: 66728
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African
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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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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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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Latino
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African
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ReadPosRankSum
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ClippingRankSum
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DP
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MQ
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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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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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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South Asian
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East Asian
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ClippingRankSum
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MQRankSum
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QD
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MQ
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FS
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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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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Other
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African
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European (Finnish)
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Latino
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East Asian
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QD
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MQ
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VQSLOD
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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Latino
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BaseQRankSum
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ReadPosRankSum
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FS
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.35e0

MQRankSum
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SIO_000300: -2.1e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.227e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.730801e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3370
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-2

ClippingRankSum
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SIO_000300: 7.71e-1

BaseQRankSum
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QD
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VQSLOD
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SIO_000300: 1.14e-1

DP
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SIO_000300: 1.730372e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 7.913e0

GenotypeDepth
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
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

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

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

East Asian
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allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.731e0

ClippingRankSum
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SIO_000300: 5.92e-1

VQSLOD
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DP
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SIO_000300: 1.730399e6

MQ
type: SiteQuality
SIO_000300: 5.931e1

QD
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SIO_000300: 1.291e1

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

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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variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.315886984715146e-4
allele num: 8636
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.298e1

FS
type: SiteQuality
SIO_000300: 8.38e-1

BaseQRankSum
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MQ
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SIO_000300: 5.917e1

DP
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SIO_000300: 1.730621e6

MQRankSum
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ClippingRankSum
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SIO_000300: -9.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.95e-1

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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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: 14

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 10
allele frequency: 8.658008658008658e-4
allele num: 11550
num of homozygotes: 0

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

East Asian
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BaseQRankSum
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SIO_000300: -7.63e-1

QD
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InbreedingCoeff
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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DP
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 6.74e-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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bin: 6.75e1
variant carriers: 0

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

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

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

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

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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East Asian
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MQ
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DP
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 9.609840476648087e-5
allele num: 10406
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European (Non-Finnish)
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allele count: 12
allele frequency: 1.79829162295819e-4
allele num: 66730
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FS
type: SiteQuality
SIO_000300: 5.29e-1

ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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DP
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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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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
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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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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Latino
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African
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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QD
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DP
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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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Other
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66646
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Latino
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African
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BaseQRankSum
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SIO_000300: 1.89e0

ReadPosRankSum
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VQSLOD
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MQ
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FS
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MQRankSum
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DP
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QD
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ClippingRankSum
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SIO_000300: -4.2e-1

InbreedingCoeff
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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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European (Finnish)
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66452
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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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South Asian
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BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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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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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

European (Finnish)
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num of homozygotes: 0

South Asian
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African
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East Asian
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Other
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Latino
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European (Non-Finnish)
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MQ
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MQRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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QD
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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Latino
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East Asian
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South Asian
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MQRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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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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East Asian
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European (Finnish)
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Latino
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Other
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African
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European (Non-Finnish)
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South Asian
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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DP
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MQRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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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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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8534
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.006957452502007e-4
allele num: 14948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65840
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.913752913752914e-4
allele num: 10296
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: 888
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

DP
type: SiteQuality
SIO_000300: 1.685754e6

MQRankSum
type: SiteQuality
SIO_000300: -2.01e0

FS
type: SiteQuality
SIO_000300: 3.202e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.95e-1

QD
type: SiteQuality
SIO_000300: 1.72e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-2

MQ
type: SiteQuality
SIO_000300: 5.694e1

GenotypeQuality
all individuals: 2791
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 922
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65370
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 7.226477814713109e-5
allele num: 13838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.735e1

VQSLOD
type: SiteQuality
SIO_000300: -1.368e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

MQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.746e0

DP
type: SiteQuality
SIO_000300: 1.661955e6

FS
type: SiteQuality
SIO_000300: 2.206e0

GenotypeQuality
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bin: 1.75e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 17

GenotypeQuality
all individuals: 8424
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.299270072992701e-5
allele num: 13700
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.082038166437143e-3
allele num: 10166
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.745200698080279e-4
allele num: 11460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.594321418726454e-5
allele num: 65298
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-2

MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 7.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.29e-2

DP
type: SiteQuality
SIO_000300: 1.658273e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

QD
type: SiteQuality
SIO_000300: 1.493e1

VQSLOD
type: SiteQuality
SIO_000300: 3.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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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: 917
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31457
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.596475235490732e-5
allele num: 13164
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65068
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 9.795e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.37e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.244e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.49e-1

DP
type: SiteQuality
SIO_000300: 1.646762e6

GenotypeQuality
all individuals: 661
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variant carriers: 0

GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 113
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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
all individuals: 2219
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4342
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1152
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.63263226165107e-5
allele num: 64758
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.579e0

QD
type: SiteQuality
SIO_000300: 1.724e1

VQSLOD
type: SiteQuality
SIO_000300: -3.764e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.635024e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12062
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.185677021579322e-4
allele num: 8434
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.925e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 1.625851e6

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -6.277e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.766e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.507742045261188e-5
allele num: 11754
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64298
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.621706e6

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 1.83e1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-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: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.202212070209185e-4
allele num: 8318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63306
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.15e-1

FS
type: SiteQuality
SIO_000300: 4.381e0

QD
type: SiteQuality
SIO_000300: 1.232e1

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

DP
type: SiteQuality
SIO_000300: 1.561808e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.463e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-2

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7622
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63140
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.015434606011373e-4
allele num: 9848
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.632e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.134e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

QD
type: SiteQuality
SIO_000300: 6.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.543582e6

GenotypeQuality
all individuals: 3596
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 3063
bin: 3.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.075731497418244e-4
allele num: 9296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.071e1

DP
type: SiteQuality
SIO_000300: 1.468364e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

GenotypeQuality
all individuals: 1060
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
all individuals: 2143
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variant carriers: 0

GenotypeQuality
all individuals: 3103
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.122082585278277e-4
allele num: 62384
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

FS
type: SiteQuality
SIO_000300: 1.199e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.85e-1

DP
type: SiteQuality
SIO_000300: 1.460622e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.88e-1

QD
type: SiteQuality
SIO_000300: 1.34e1

GenotypeQuality
all individuals: 10093
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variant carriers: 0

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

GenotypeQuality
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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
all individuals: 1719
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variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.615091414174042e-5
allele num: 61916
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.282e0

MQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

MQ
type: SiteQuality
SIO_000300: 5.829e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

QD
type: SiteQuality
SIO_000300: 4.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

DP
type: SiteQuality
SIO_000300: 1.454998e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1929
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variant carriers: 15

GenotypeQuality
all individuals: 1363
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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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: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 1003
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variant carriers: 5

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 66
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variant carriers: 2

GenotypeQuality
all individuals: 1472
bin: 6.25e1
variant carriers: 6

European (Finnish)
type: Population
allele count: 325
allele frequency: 4.916792738275341e-2
allele num: 6610
num of homozygotes: 5

South Asian
type: Population
allele count: 2432
allele frequency: 1.473760756271967e-1
allele num: 16502
num of homozygotes: 191

African
type: Population
allele count: 1043
allele frequency: 1.002884615384615e-1
allele num: 10400
num of homozygotes: 55

European (Non-Finnish)
type: Population
allele count: 5248
allele frequency: 7.870425914817036e-2
allele num: 66680
num of homozygotes: 196

Other
type: Population
allele count: 110
allele frequency: 1.211453744493392e-1
allele num: 908
num of homozygotes: 5

Latino
type: Population
allele count: 2339
allele frequency: 2.026511869693294e-1
allele num: 11542
num of homozygotes: 250

East Asian
type: Population
allele count: 2038
allele frequency: 2.365915950777804e-1
allele num: 8614
num of homozygotes: 261

ClippingRankSum
type: SiteQuality
SIO_000300: -3.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.71e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.18e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.826e0

DP
type: SiteQuality
SIO_000300: 3.470905e6

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 100
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GenotypeQuality
all individuals: 2150
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
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: 10404
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 7.84e-1

QD
type: SiteQuality
SIO_000300: 1.381e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.244e0

DP
type: SiteQuality
SIO_000300: 3.422425e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.497e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.341e1

VQSLOD
type: SiteQuality
SIO_000300: -1.283e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.822e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 3.422988e6

MQRankSum
type: SiteQuality
SIO_000300: -1.345e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.109e0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1965
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 2386
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GenotypeQuality
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GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 1202
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GenotypeQuality
all individuals: 47673
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99868058054456e-5
allele num: 66696
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.763e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

FS
type: SiteQuality
SIO_000300: 1.966e0

DP
type: SiteQuality
SIO_000300: 3.424233e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

QD
type: SiteQuality
SIO_000300: 1.529e1

GenotypeQuality
all individuals: 2149
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2387
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.384e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.78e-1

DP
type: SiteQuality
SIO_000300: 3.424605e6

MQ
type: SiteQuality
SIO_000300: 5.981e1

MQRankSum
type: SiteQuality
SIO_000300: 9.28e-1

QD
type: SiteQuality
SIO_000300: 1.13e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.81e-1

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2389
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47678
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.009e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

DP
type: SiteQuality
SIO_000300: 3.425431e6

VQSLOD
type: SiteQuality
SIO_000300: 6.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.39e-1

QD
type: SiteQuality
SIO_000300: 1.253e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.55e-1

GenotypeQuality
all individuals: 1212
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2156
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variant carriers: 0

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

GenotypeQuality
all individuals: 2390
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variant carriers: 0

GenotypeQuality
all individuals: 1894
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variant carriers: 0

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

GenotypeQuality
all individuals: 2100
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1674
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variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.265e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: -1.44e-1

FS
type: SiteQuality
SIO_000300: 8.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 3.425981e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

MQRankSum
type: SiteQuality
SIO_000300: -1.235e0

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2060
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
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variant carriers: 0

GenotypeQuality
all individuals: 1819
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variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 114
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1160
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47110
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2323
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16394
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66488
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.461468e6

MQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

QD
type: SiteQuality
SIO_000300: 2.17e0

MQ
type: SiteQuality
SIO_000300: 5.992e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.26e-1

FS
type: SiteQuality
SIO_000300: 1.652e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.81e-2

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1964
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 51
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 123
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variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 153
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1457
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.016123210203345e-5
allele num: 66488
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.482702577199907e-4
allele num: 8614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.09979260705136e-5
allele num: 16394
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.81e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.26e-1

FS
type: SiteQuality
SIO_000300: 1.652e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 3.461468e6

QD
type: SiteQuality
SIO_000300: 2.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

MQ
type: SiteQuality
SIO_000300: 5.992e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
all individuals: 1235
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variant carriers: 0

GenotypeQuality
all individuals: 2409
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variant carriers: 0

GenotypeQuality
all individuals: 1716
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variant carriers: 0

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

GenotypeQuality
all individuals: 1930
bin: 7.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 1.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.145e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.41e0

QD
type: SiteQuality
SIO_000300: 1.201e1

DP
type: SiteQuality
SIO_000300: 3.434333e6