X-105139451-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105139451
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105139451
    reference: chr 0
allele count: 1
allele frequency: 1.152060460132948e-5
allele num: 86801
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.515G>A
  hgvsp: ENSP00000434830.1:p.Arg172Gln
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.515G>A
  hgvsp: ENSP00000438378.1:p.Arg172Gln
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Arg172Gln
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4519
  num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

X-105139509-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105139509
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105139509
    reference: chr 0
allele count: 3
allele frequency: 3.491742030098816e-5
allele num: 85917
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.573A>T
  hgvsp: ENST00000243300.9:c.573A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.573A>T
  hgvsp: ENST00000428173.2:c.573A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Val191Val
num of homozygotes: 0
population: African
  type: Population
  allele count: 3
  allele frequency: 3.80952380952381e-4
  allele num: 7875
  num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

X-105139520-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105139520
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105139520
    reference: chr 0
allele count: 1
allele frequency: 1.173295787868122e-5
allele num: 85230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.580+4A>C
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.580+4A>C
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6556
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: c.580+4A>C
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9151
  num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-105139526-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105139526
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105139526
    reference: chr 0
allele count: 1
allele frequency: 1.180122024617345e-5
allele num: 84737
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.580+10T>C
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.580+10T>C
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
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  allele frequency: 0.0e0
  allele num: 9319
  num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

X-105139555-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105139555
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105139555
    reference: chr 0
allele count: 1
allele frequency: 1.218279059001255e-5
allele num: 82083
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.580+39T>G
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.580+39T>G
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
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  allele num: 4355
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population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD

X-105139558-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
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    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105139558
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 81550
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.580+42A>G
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.580+42A>G
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
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  allele num: 7680
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD

X-105139564-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105139564
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105139564
    reference: chr 0
allele count: 1
allele frequency: 1.244617031339457e-5
allele num: 80346
alternate allele: G
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.580+48A>G
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.580+48A>G
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Latino
population: African
population: Other
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population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

X-105142530-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142530
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142530
    reference: chr 0
allele count: 1
allele frequency: 2.235586058885337e-5
allele num: 44731
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.581-47C>T
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.581-47C>T
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
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  allele num: 2637
  num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

X-105142555-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142555
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142555
    reference: chr 0
allele count: 1
allele frequency: 2.09608451412761e-5
allele num: 47708
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.581-22G>A
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.581-22G>A
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 572
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
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  allele frequency: 0.0e0
  allele num: 3573
  num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

X-105142573-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142573
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142573
    reference: chr 0
allele count: 1
allele frequency: 1.862162715778105e-5
allele num: 53701
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.581-4G>T
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.581-4G>T
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.581-4G>T
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.685487948761166e-4
  allele num: 5933
  num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

X-105142576-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142576
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142576
    reference: chr 0
allele count: 1
allele frequency: 1.82618382366369e-5
allele num: 54759
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.581-1G>A
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.581-1G>A
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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population: Other
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  allele frequency: 0.0e0
  allele num: 414
  num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
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X-105142603-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142603
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142603
    reference: chr 0
allele count: 15
allele frequency: 2.541898967989019e-4
allele num: 59011
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.607A>T
  hgvsp: ENSP00000438378.1:p.Ser203Cys
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.607A>T
  hgvsp: ENSP00000434830.1:p.Ser203Cys
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: European (Non-Finnish)
  type: Population
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population: European (Finnish)
population: African
population: East Asian
population: Other
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population: South Asian
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site quality: DP
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site quality: FS
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X-105142630-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142630
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142630
    reference: chr 0
allele count: 1
allele frequency: 1.69284940411701e-5
allele num: 59072
alternate allele: A
annotation: Annotation
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  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.634T>A
  hgvsp: ENSP00000438378.1:p.Phe212Ile
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.634T>A
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  variant of: http://identifiers.org/hgnc/25391
canonical: true
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe212Ile
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6275
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

X-105142634-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142634
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142634
    reference: chr 0
allele count: 23
allele frequency: 3.898106875921563e-4
allele num: 59003
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.638T>C
  hgvsp: ENSP00000438378.1:p.Ile213Thr
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.638T>C
  hgvsp: ENSP00000434830.1:p.Ile213Thr
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ile213Thr
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 3
  allele frequency: 4.415660877244627e-4
  allele num: 6794
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-105142636-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142636
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142636
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 58757
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.640G>T
  hgvsp: ENSP00000438378.1:p.Gly214Trp
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.640G>T
  hgvsp: ENSP00000434830.1:p.Gly214Trp
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 533
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  variant carriers: 0
hgvs: p.Gly214Trp
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6245
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

X-105142644-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142644
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142644
    reference: chr 0
allele count: 1
allele frequency: 1.708496352360288e-5
allele num: 58531
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.648A>G
  hgvsp: ENST00000243300.9:c.648A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.648A>G
  hgvsp: ENST00000428173.2:c.648A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 530
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hgvs: p.Pro216Pro
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3061
  num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

X-105142683-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142683
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142683
    reference: chr 0
allele count: 2
allele frequency: 3.528830545557202e-5
allele num: 56676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.687C>T
  hgvsp: ENST00000243300.9:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.687C>T
  hgvsp: ENST00000428173.2:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Asp229Asp
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6630
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

X-105142690-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142690
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142690
    reference: chr 0
allele count: 45
allele frequency: 8.05513290969301e-4
allele num: 55865
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.694C>T
  hgvsp: ENSP00000438378.1:p.Arg232Cys
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.694C>T
  hgvsp: ENSP00000434830.1:p.Arg232Cys
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg232Cys
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2903
  num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

X-105142691-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142691
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142691
    reference: chr 0
allele count: 1
allele frequency: 1.795815749304122e-5
allele num: 55685
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.695G>A
  hgvsp: ENSP00000438378.1:p.Arg232His
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.695G>A
  hgvsp: ENSP00000434830.1:p.Arg232His
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg232His
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 1.5220700152207e-4
  allele num: 6570
  num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

X-105142725-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142725
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142725
    reference: chr 0
allele count: 1
allele frequency: 1.980550989285219e-5
allele num: 50491
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.711+18G>A
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.711+18G>A
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5568
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-105142729-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142729
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142729
    reference: chr 0
allele count: 1
allele frequency: 2.012436859793524e-5
allele num: 49691
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.711+22G>T
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.711+22G>T
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2667
  num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

X-105142730-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142730
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105142730
    reference: chr 0
allele count: 6
allele frequency: 1.21036068748487e-4
allele num: 49572
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.711+23T>C
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.711+23T>C
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
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  allele num: 355
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population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQ
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X-105142735-A-C
type: Variant
location: Region
  begin: Position
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    reference: chr 0
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    type: ExactPosition
    position: 24105142735
    reference: chr 0
allele count: 1
allele frequency: 2.0671834625323e-5
allele num: 48375
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
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  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.711+28A>C
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: European (Non-Finnish)
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population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
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site quality: ReadPosRankSum
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X-105142749-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105142749
    reference: chr 0
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    type: ExactPosition
    position: 24105142749
    reference: chr 0
allele count: 3
allele frequency: 7.296429613775658e-5
allele num: 41116
alternate allele: T
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000123572
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  gene symbol: NRK
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  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.711+42A>T
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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population: Latino
population: South Asian
population: European (Finnish)
population: Other
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population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
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X-105144583-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105144583
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105144583
    reference: chr 0
allele count: 1
allele frequency: 2.39377618192699e-5
allele num: 41775
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.712-28G>T
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.712-28G>T
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Other
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population: Latino
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population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
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X-105144588-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105144588
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105144588
    reference: chr 0
allele count: 1
allele frequency: 2.331382743104936e-5
allele num: 42893
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.712-23T>G
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.712-23T>G
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 22588
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

X-105144597-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105144597
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105144597
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 46788
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.712-14C>G
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.712-14C>G
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5194
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ

X-105144613-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105144613
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105144613
    reference: chr 0
allele count: 8
allele frequency: 1.551560287814433e-4
allele num: 51561
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.714T>C
  hgvsp: ENST00000428173.2:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.714T>C
  hgvsp: ENST00000243300.9:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.714T>C
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-105144638-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105144638
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105144638
    reference: chr 0
allele count: 1
allele frequency: 1.910840196434372e-5
allele num: 52333
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.739G>A
  hgvsp: ENSP00000438378.1:p.Ala247Thr
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.739G>A
  hgvsp: ENSP00000434830.1:p.Ala247Thr
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ala247Thr
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2878
  num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-105144639-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105144639
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105144639
    reference: chr 0
allele count: 2
allele frequency: 3.832959619770406e-5
allele num: 52179
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.740C>T
  hgvsp: ENSP00000434830.1:p.Ala247Val
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.740C>T
  hgvsp: ENSP00000438378.1:p.Ala247Val
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala247Val
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 391
  num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

X-105144679-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105144679
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105144678
    reference: chr 0
allele count: 1
allele frequency: 2.572082615293603e-5
allele num: 38879
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.766+17delT
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.766+17delT
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5424
  num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: GT
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

X-105144687-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105144687
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105144687
    reference: chr 0
allele count: 1
allele frequency: 2.798063739891995e-5
allele num: 35739
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.766+22T>C
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.766+22T>C
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 315
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-105144696-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105144696
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105144696
    reference: chr 0
allele count: 4
allele frequency: 1.243123970537962e-4
allele num: 32177
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.766+31G>T
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.766+31G>T
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18019
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4918
  num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-105144711-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105144711
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105144710
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 26629
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.766+47delT
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.766+47delT
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 19726
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3307
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: CT
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-105144712-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105144712
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105144712
    reference: chr 0
allele count: 1
allele frequency: 3.734269390193809e-5
allele num: 26779
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.766+47T>G
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.766+47T>G
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
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genotype depth: GenotypeDepth
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population: African
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population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

X-105149223-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149223
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105149223
    reference: chr 0
allele count: 1
allele frequency: 1.952819871895016e-5
allele num: 51208
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.767-35T>G
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.767-35T>G
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Other
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  allele num: 391
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population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
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X-105149234-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149234
    reference: chr 0
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    type: ExactPosition
    position: 24105149234
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 53744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
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  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.767-24A>C
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
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  hgvsc: ENST00000428173.2:c.767-24A>C
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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population: African
population: Other
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population: South Asian
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reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
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X-105149240-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149240
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105149240
    reference: chr 0
allele count: 20
allele frequency: 3.582495924910885e-4
allele num: 55827
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.767-18A>G
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.767-18A>G
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: African
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population: South Asian
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site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
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site quality: InbreedingCoeff
site quality: MQ
site quality: FS
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site quality: QD
site quality: DP

X-105149241-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149241
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105149241
    reference: chr 0
allele count: 1
allele frequency: 1.780056249777493e-5
allele num: 56178
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
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  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.767-17T>C
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.767-17T>C
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 29746
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD

X-105149244-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149244
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105149244
    reference: chr 0
allele count: 40
allele frequency: 6.967548642198958e-4
allele num: 57409
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.767-14A>G
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.767-14A>G
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3073
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

X-105149261-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149261
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105149261
    reference: chr 0
allele count: 1
allele frequency: 1.543948493878244e-5
allele num: 64769
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.770T>C
  hgvsp: ENSP00000438378.1:p.Leu257Pro
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.770T>C
  hgvsp: ENSP00000434830.1:p.Leu257Pro
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Leu257Pro
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 472
  num of homozygotes: 0
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: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-105149264-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149264
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105149265
    reference: chr 0
allele count: 1
allele frequency: 1.526531110704036e-5
allele num: 65508
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.774dupT
  hgvsp: ENSP00000434830.1:p.Asn259Ter
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.774dupT
  hgvsp: ENSP00000438378.1:p.Asn259Ter
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 616
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  variant carriers: 0
genotype depth: GenotypeDepth
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hgvs: p.Asn259Ter
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 477
  num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
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site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
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site quality: BaseQRankSum

X-105149292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149292
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105149292
    reference: chr 0
allele count: 2
allele frequency: 2.948721729130422e-5
allele num: 67826
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.801C>T
  hgvsp: ENST00000428173.2:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.801C>T
  hgvsp: ENST00000243300.9:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Phe267Phe
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7411
  num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

X-105149303-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149303
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105149303
    reference: chr 0
allele count: 2
allele frequency: 2.981825771920147e-5
allele num: 67073
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.812G>A
  hgvsp: ENSP00000434830.1:p.Arg271Gln
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.812G>A
  hgvsp: ENSP00000438378.1:p.Arg271Gln
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Arg271Gln
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 484
  num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

X-105149331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149331
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105149331
    reference: chr 0
allele count: 7
allele frequency: 1.157369134618564e-4
allele num: 60482
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.840C>T
  hgvsp: ENST00000428173.2:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.840C>T
  hgvsp: ENST00000243300.9:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13498
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Ser280Ser
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.56128024980484e-4
  allele num: 6405
  num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-105149332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149332
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105149332
    reference: chr 0
allele count: 25
allele frequency: 4.176202328650419e-4
allele num: 59863
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.841G>A
  hgvsp: ENSP00000434830.1:p.Gly281Arg
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.841G>A
  hgvsp: ENSP00000438378.1:p.Gly281Arg
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10658
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Gly281Arg
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6163
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

X-105149339-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149339
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105149339
    reference: chr 0
allele count: 1
allele frequency: 1.709810894915022e-5
allele num: 58486
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.845+3A>G
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.845+3A>G
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.845+3A>G
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 3.195398625978591e-5
  allele num: 31295
  num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS

X-105149347-A-G
type: Variant
location: Region
  begin: Position
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site quality: MQRankSum
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X-105149359-C-T
type: Variant
location: Region
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allele count: 1
allele frequency: 1.87765218370949e-5
allele num: 53258
alternate allele: T
annotation: Annotation
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  gene symbol: NRK
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  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
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  consequence: intron_variant
  ensembl gene: ENSG00000123572
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  ensembl transcript: ENST00000243300
  gene symbol: NRK
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  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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X-105149360-C-A
type: Variant
location: Region
  begin: Position
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    position: 24105149360
    reference: chr 0
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allele count: 1
allele frequency: 1.888181869677687e-5
allele num: 52961
alternate allele: A
annotation: Annotation
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  gene symbol: NRK
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  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
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  variant of: http://identifiers.org/hgnc/25391
canonical: true
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X-105149372-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149372
    reference: chr 0
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allele count: 2
allele frequency: 4.065784391453721e-5
allele num: 49191
alternate allele: T
annotation: Annotation
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  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
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  ensembl gene: ENSG00000123572
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  ensembl transcript: ENST00000243300
  gene symbol: NRK
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  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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X-105149373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105149373
    reference: chr 0
  end: Position
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allele count: 33
allele frequency: 6.764651620441547e-4
allele num: 48783
alternate allele: T
annotation: Annotation
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  gene symbol: NRK
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  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
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  ensembl gene: ENSG00000123572
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  gene symbol: NRK
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  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
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  allele num: 5522
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population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
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X-105149379-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
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    reference: chr 0
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    type: ExactPosition
    position: 24105149379
    reference: chr 0
allele count: 2
allele frequency: 4.303018567525119e-5
allele num: 46479
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
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  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.845+43A>G
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.845+43A>G
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: African
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  allele num: 5321
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population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
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X-105150361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150361
    reference: chr 0
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    type: ExactPosition
    position: 24105150361
    reference: chr 0
allele count: 4
allele frequency: 2.294104152328516e-4
allele num: 17436
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.846-46C>T
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.846-46C>T
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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population: Other
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population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
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site quality: VQSLOD
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site quality: QD
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X-105150365-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150365
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150365
    reference: chr 0
allele count: 1
allele frequency: 5.608524957936063e-5
allele num: 17830
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.846-42A>T
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.846-42A>T
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: African
population: European (Non-Finnish)
population: East Asian
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population: Latino
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site quality: QD
site quality: ClippingRankSum
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X-105150375-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150375
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150376
    reference: chr 0
allele count: 6
allele frequency: 3.305420890260026e-4
allele num: 18152
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.846-24dupT
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.846-24dupT
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 8.312551953449709e-4
  allele num: 1203
  num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

X-105150375-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150375
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150374
    reference: chr 0
allele count: 3
allele frequency: 1.652710445130013e-4
allele num: 18152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.846-24delT
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.846-24delT
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1203
  num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: CT
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

X-105150383-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150383
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150383
    reference: chr 0
allele count: 6
allele frequency: 2.815843814529754e-4
allele num: 21308
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.846-24T>C
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.846-24T>C
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
  type: Population
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  allele frequency: 7.776049766718507e-4
  allele num: 1286
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

X-105150389-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150389
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150387
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 22917
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.846-16_846-15delTT
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.846-16_846-15delTT
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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population: European (Finnish)
  type: Population
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  allele frequency: 0.0e0
  allele num: 1772
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: CTT
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD

X-105150390-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150390
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150390
    reference: chr 0
allele count: 3
allele frequency: 1.284961665310318e-4
allele num: 23347
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.846-17T>C
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.846-17T>C
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17850
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD

X-105150398-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150398
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150399
    reference: chr 0
allele count: 1
allele frequency: 3.888780867198134e-5
allele num: 25715
alternate allele: AT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.846-3dupT
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.846-3dupT
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 4.380201489268506e-4
  allele num: 2283
  num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

X-105150411-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150411
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150411
    reference: chr 0
allele count: 1
allele frequency: 3.324247058041354e-5
allele num: 30082
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.850C>T
  hgvsp: ENSP00000438378.1:p.Arg284Cys
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.850C>T
  hgvsp: ENSP00000434830.1:p.Arg284Cys
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg284Cys
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2006
  num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

X-105150435-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150435
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150435
    reference: chr 0
allele count: 1
allele frequency: 2.569241046194954e-5
allele num: 38922
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.874A>G
  hgvsp: ENSP00000438378.1:p.Lys292Glu
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.874A>G
  hgvsp: ENSP00000434830.1:p.Lys292Glu
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3766
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Lys292Glu
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4674
  num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

X-105150440-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150440
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150440
    reference: chr 0
allele count: 1
allele frequency: 2.508654859264463e-5
allele num: 39862
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.879T>C
  hgvsp: ENST00000243300.9:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.879T>C
  hgvsp: ENST00000428173.2:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Cys293Cys
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 20986
  num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-105150442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150442
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150442
    reference: chr 0
allele count: 1
allele frequency: 2.486139770777913e-5
allele num: 40223
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.881C>T
  hgvsp: ENSP00000434830.1:p.Thr294Met
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.881C>T
  hgvsp: ENSP00000438378.1:p.Thr294Met
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 99
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr294Met
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2307
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

X-105150470-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150470
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150470
    reference: chr 0
allele count: 2
allele frequency: 4.548866195100871e-5
allele num: 43967
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.909T>A
  hgvsp: ENST00000243300.9:c.909T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.909T>A
  hgvsp: ENST00000428173.2:c.909T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 211
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  variant carriers: 0
hgvs: p.Thr303Thr
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2396
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS

X-105150494-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150494
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150494
    reference: chr 0
allele count: 8
allele frequency: 1.782054709079569e-4
allele num: 44892
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.933A>G
  hgvsp: ENST00000243300.9:c.933A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.933A>G
  hgvsp: ENST00000428173.2:c.933A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 310
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  variant carriers: 0
hgvs: p.Pro311Pro
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6135
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

X-105150501-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150501
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150501
    reference: chr 0
allele count: 1
allele frequency: 2.245021664459062e-5
allele num: 44543
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.940C>A
  hgvsp: ENST00000428173.2:c.940C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.940C>A
  hgvsp: ENST00000243300.9:c.940C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 693
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg314Arg
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3472
  num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

X-105150502-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150502
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150502
    reference: chr 0
allele count: 5
allele frequency: 1.12200704620425e-4
allele num: 44563
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.941G>A
  hgvsp: ENSP00000438378.1:p.Arg314Gln
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.941G>A
  hgvsp: ENSP00000434830.1:p.Arg314Gln
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 26536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 2.75e1
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genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg314Gln
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5086
  num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

X-105150512-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150512
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150512
    reference: chr 0
allele count: 1
allele frequency: 2.253521126760563e-5
allele num: 44375
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.951A>C
  hgvsp: ENSP00000434830.1:p.Lys317Asn
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.951A>C
  hgvsp: ENSP00000438378.1:p.Lys317Asn
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys317Asn
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 4.334257975034674e-5
  allele num: 23072
  num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

X-105150517-AACG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150517
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150514
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 44139
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.959_961delGAC
  hgvsp: ENSP00000438378.1:p.Arg320del
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.959_961delGAC
  hgvsp: ENSP00000434830.1:p.Arg320del
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: inframe deletion
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Arg320del
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 340
  num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: AACG
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

X-105150531-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150531
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150531
    reference: chr 0
allele count: 1
allele frequency: 2.344281126192653e-5
allele num: 42657
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.970G>A
  hgvsp: ENSP00000434830.1:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.970G>A
  hgvsp: ENSP00000438378.1:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5978
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 454
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  variant carriers: 0
hgvs: p.Glu324Lys
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2293
  num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

X-105150535-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150535
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150535
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 42147
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.974C>A
  hgvsp: ENSP00000438378.1:p.Ser325Ter
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.974C>A
  hgvsp: ENSP00000434830.1:p.Ser325Ter
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Ser325Ter
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2277
  num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

X-105150537-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150537
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150537
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 41897
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.976T>C
  hgvsp: ENST00000243300.9:c.976T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.976T>C
  hgvsp: ENST00000428173.2:c.976T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Leu326Leu
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5735
  num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

X-105150541-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150541
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150541
    reference: chr 0
allele count: 2
allele frequency: 4.851895878314451e-5
allele num: 41221
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.980C>T
  hgvsp: ENSP00000434830.1:p.Thr327Ile
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.980C>T
  hgvsp: ENSP00000438378.1:p.Thr327Ile
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Thr327Ile
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2225
  num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
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X-105150545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150545
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150545
    reference: chr 0
allele count: 1
allele frequency: 2.505888838771112e-5
allele num: 39906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.984G>A
  hgvsp: ENST00000243300.9:c.984G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.984G>A
  hgvsp: ENST00000428173.2:c.984G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1179
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  variant carriers: 1
genotype depth: GenotypeDepth
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hgvs: p.Arg328Arg
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3393
  num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
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site quality: MQ

X-105150560-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150560
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150560
    reference: chr 0
allele count: 1
allele frequency: 2.788777957499024e-5
allele num: 35858
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.999C>T
  hgvsp: ENST00000428173.2:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.999C>T
  hgvsp: ENST00000243300.9:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1836
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile333Ile
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2048
  num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

X-105150565-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24105150565
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24105150565
    reference: chr 0
allele count: 1
allele frequency: 2.923036450264535e-5
allele num: 34211
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000438378
  ensembl transcript: ENST00000428173
  gene symbol: NRK
  hgvsc: ENST00000428173.2:c.1004A>C
  hgvsp: ENSP00000438378.1:p.Lys335Thr
  variant of: http://identifiers.org/hgnc/25391
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123572
  ensembl protein: ENSP00000434830
  ensembl transcript: ENST00000243300
  gene symbol: NRK
  hgvsc: ENST00000243300.9:c.1004A>C
  hgvsp: ENSP00000434830.1:p.Lys335Thr
  variant of: http://identifiers.org/hgnc/25391
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8941
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14826
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6631
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1835
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys335Thr
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 1
  allele frequency: 3.665689149560117e-4
  allele num: 2728
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10071
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.088772845953003e-5
allele num: 47875
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-2

FS
type: SiteQuality
SIO_000300: 4.292e0

QD
type: SiteQuality
SIO_000300: 1.407e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e0

DP
type: SiteQuality
SIO_000300: 1.715903e6

MQ
type: SiteQuality
SIO_000300: 5.94e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.387e0

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9689
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 611
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

QD
type: SiteQuality
SIO_000300: 1.385e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.209e-1

MQ
type: SiteQuality
SIO_000300: 5.847e1

DP
type: SiteQuality
SIO_000300: 1.690117e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.88e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

African
type: Population
allele count: 1
allele frequency: 1.273885350318471e-4
allele num: 7850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4462
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9463
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47187
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.357e0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

MQ
type: SiteQuality
SIO_000300: 5.849e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 2.66e0

QD
type: SiteQuality
SIO_000300: 6.93e0

DP
type: SiteQuality
SIO_000300: 1.658053e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.71e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4447
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.278935925310142e-4
allele num: 7819
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9129
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6477
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46940
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.015e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

QD
type: SiteQuality
SIO_000300: 1.153e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.82e-1

DP
type: SiteQuality
SIO_000300: 1.627514e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6237
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8983
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7704
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 587
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.192934365474441e-5
allele num: 45601
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.769e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.430209e6

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45327
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6184
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 583
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.415829e6

QD
type: SiteQuality
SIO_000300: 2.721e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.66e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8859
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.238538681948424e-5
allele num: 44672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8243
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.403879e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.25e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.728e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.813e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3262
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3921
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23379
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5126
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.652619401751777e-4
allele num: 6051
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 355
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.949e1

DP
type: SiteQuality
SIO_000300: 8.73488e5

VQSLOD
type: SiteQuality
SIO_000300: 7.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.99e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5402
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.604363869725654e-4
allele num: 6233
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25003
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 377
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.874e-1

DP
type: SiteQuality
SIO_000300: 9.79586e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

QD
type: SiteQuality
SIO_000300: 2.954e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2936
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: -1.056e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.89e-1

FS
type: SiteQuality
SIO_000300: 4.693e0

QD
type: SiteQuality
SIO_000300: 8.94e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.147e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

DP
type: SiteQuality
SIO_000300: 1.079437e6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5985
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.322880371660859e-4
allele num: 4305
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28959
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5521
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.096e0

QD
type: SiteQuality
SIO_000300: 7.56e0

MQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.5e-3

DP
type: SiteQuality
SIO_000300: 1.093804e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.352e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.102e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3136
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6302
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4706
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.272727272727273e-3
allele num: 440
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 2.253339771446966e-3
allele num: 6213
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6794
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.68e-1

DP
type: SiteQuality
SIO_000300: 1.140452e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

FS
type: SiteQuality
SIO_000300: 5.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

QD
type: SiteQuality
SIO_000300: 1.276e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4713
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3092
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31463
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6307
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.472320376914016e-4
allele num: 6792
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.857e1

DP
type: SiteQuality
SIO_000300: 1.12564e6

VQSLOD
type: SiteQuality
SIO_000300: -1.213e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 2.229299363057325e-4
allele num: 31400
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 9.569377990430622e-4
allele num: 6270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 6.457862447529867e-4
allele num: 3097
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 8.479966080135679e-4
allele num: 4717
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.587553579933323e-4
allele num: 6299
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.73e-1

DP
type: SiteQuality
SIO_000300: 1.121912e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-1

QD
type: SiteQuality
SIO_000300: 1.651e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.28e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3080
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6263
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31273
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.251e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 1.119978e6

VQSLOD
type: SiteQuality
SIO_000300: -3.21e0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6769
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6243
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4701
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6231
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.215537477089296e-5
allele num: 31099
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 427
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.108882e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e-1

QD
type: SiteQuality
SIO_000300: 7.24e0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.327676283651126e-5
allele num: 30051
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5995
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6107
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.388681802778719e-4
allele num: 2951
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 413
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 1.087924e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.92e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

South Asian
type: Population
allele count: 43
allele frequency: 6.526028228866292e-3
allele num: 6589
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.657000828500414e-4
allele num: 6035
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4447
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.375185635209936e-5
allele num: 29628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 401
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.075042e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

FS
type: SiteQuality
SIO_000300: 6.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.539e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.65e-2

QD
type: SiteQuality
SIO_000300: 1.983e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6027
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4437
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29545
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5816
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.493e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

DP
type: SiteQuality
SIO_000300: 1.072185e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.733154141934521e-5
allele num: 26787
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 359
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2693
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3952
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.127e0

VQSLOD
type: SiteQuality
SIO_000300: 8.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

FS
type: SiteQuality
SIO_000300: 4.533e0

QD
type: SiteQuality
SIO_000300: 1.45e1

MQ
type: SiteQuality
SIO_000300: 5.985e1

DP
type: SiteQuality
SIO_000300: 9.26308e5

BaseQRankSum
type: SiteQuality
SIO_000300: -6.859e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.71e-2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3887
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.670564650851988e-4
allele num: 5986
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5517
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.287e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.382e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.82e-2

DP
type: SiteQuality
SIO_000300: 9.01505e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5991
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26253
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3878
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.02757502027575e-4
allele num: 4932
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 9.082652134423251e-4
allele num: 5505
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VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

QD
type: SiteQuality
SIO_000300: 1.15e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.9519e5

MQRankSum
type: SiteQuality
SIO_000300: -2.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.85e-2

FS
type: SiteQuality
SIO_000300: 4.698e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.323e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

African
type: Population
allele count: 1
allele frequency: 1.851851851851852e-4
allele num: 5400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4767
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3773
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5871
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.71e0

DP
type: SiteQuality
SIO_000300: 8.59858e5

MQRankSum
type: SiteQuality
SIO_000300: 3.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.739e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3827
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 1.277683134582623e-3
allele num: 2348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 309
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21568
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.377e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.82141e5

FS
type: SiteQuality
SIO_000300: 1.551e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.01e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

QD
type: SiteQuality
SIO_000300: 1.333e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 339
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4766
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.813731007315701e-4
allele num: 3554
num of homozygotes: 0

East Asian
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
allele num: 5434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22050
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.875e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.68e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.781e0

VQSLOD
type: SiteQuality
SIO_000300: -7.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

DP
type: SiteQuality
SIO_000300: 1.024534e6

QD
type: SiteQuality
SIO_000300: 7.33e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2569
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4873
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.10077519379845e-4
allele num: 3225
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 1.050732e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.66e-1

QD
type: SiteQuality
SIO_000300: 7.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.47e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.115e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2679
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5935
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 371
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24673
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

QD
type: SiteQuality
SIO_000300: 3.026e1

DP
type: SiteQuality
SIO_000300: 1.135438e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4012
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.958480219349785e-4
allele num: 5106
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27349
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 1.2531328320802e-3
allele num: 5586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2832
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.27e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.301e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e-1

DP
type: SiteQuality
SIO_000300: 1.202938e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.95e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4088
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.607113227284205e-5
allele num: 27723
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5629
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5225
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
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MQ
type: SiteQuality
SIO_000300: 5.866e1

FS
type: SiteQuality
SIO_000300: 1.527e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.205053e6

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: -1.73e0

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5191
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2869
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South Asian
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4072
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 5622
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.235366471311772e-5
allele num: 27642
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.202202e6

QD
type: SiteQuality
SIO_000300: 5.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.457e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

FS
type: SiteQuality
SIO_000300: 1.686e0

MQRankSum
type: SiteQuality
SIO_000300: 4.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

Other
type: Population
allele count: 0
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allele num: 334
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4441
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.912315174141573e-5
allele num: 20357
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2343
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3153
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2827
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MQ
type: SiteQuality
SIO_000300: 6.095e1

DP
type: SiteQuality
SIO_000300: 9.46888e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.01e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

QD
type: SiteQuality
SIO_000300: 3.213e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4161
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.377789728421619e-5
allele num: 18595
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2693
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2267
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5193
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East Asian
type: Population
allele count: 0
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allele num: 2515
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MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.234e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.52e0

QD
type: SiteQuality
SIO_000300: 1.084e1

MQ
type: SiteQuality
SIO_000300: 5.924e1

DP
type: SiteQuality
SIO_000300: 8.96998e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

FS
type: SiteQuality
SIO_000300: 1.152e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.61e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

Latino
type: Population
allele count: 4
allele frequency: 1.875293014533521e-3
allele num: 2133
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2196
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2152
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16643
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.239e1

DP
type: SiteQuality
SIO_000300: 8.56458e5

FS
type: SiteQuality
SIO_000300: 1.793e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.12e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1921
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South Asian
type: Population
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1352
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13777
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.99e-2

DP
type: SiteQuality
SIO_000300: 8.1731e5

MQ
type: SiteQuality
SIO_000300: 6.119e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.73e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

QD
type: SiteQuality
SIO_000300: 1.622e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
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South Asian
type: Population
allele count: 1
allele frequency: 2.287805994051705e-4
allele num: 4371
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1922
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13832
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.89e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.17216e5

QD
type: SiteQuality
SIO_000300: 2.855e1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4917
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5726
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.707411114818522e-5
allele num: 26973
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2860
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QD
type: SiteQuality
SIO_000300: 2.636e1

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.17e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.129165e6

FS
type: SiteQuality
SIO_000300: 0.0e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2934
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African
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6575
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28372
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MQ
type: SiteQuality
SIO_000300: 5.395e1

VQSLOD
type: SiteQuality
SIO_000300: -4.859e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

QD
type: SiteQuality
SIO_000300: 1.719e1

DP
type: SiteQuality
SIO_000300: 1.206415e6

African
type: Population
allele count: 0
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East Asian
type: Population
allele count: 20
allele frequency: 4.594532506317482e-3
allele num: 4353
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6663
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29520
num of homozygotes: 0

Latino
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allele count: 0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.055e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

QD
type: SiteQuality
SIO_000300: 2.005e1

DP
type: SiteQuality
SIO_000300: 1.250724e6

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3020
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Other
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allele count: 0
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allele num: 425
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African
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allele count: 0
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allele num: 6149
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Latino
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allele count: 0
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South Asian
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allele count: 0
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East Asian
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allele num: 4383
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QD
type: SiteQuality
SIO_000300: 2.717e1

DP
type: SiteQuality
SIO_000300: 1.255488e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.5e-2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.57116572479958e-5
allele num: 30436
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East Asian
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Latino
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allele count: 0
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South Asian
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allele count: 38
allele frequency: 5.612169546595776e-3
allele num: 6771
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African
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allele count: 0
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Other
type: Population
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allele num: 428
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

QD
type: SiteQuality
SIO_000300: 2.62e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

DP
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VQSLOD
type: SiteQuality
SIO_000300: 5.18e-1

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.18e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.882675122513693e-5
allele num: 34690
num of homozygotes: 0

African
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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East Asian
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South Asian
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MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.152e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7183
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.375515818431912e-4
allele num: 7270
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5207
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3423
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6825
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35123
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DP
type: SiteQuality
SIO_000300: 1.399679e6

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

MQ
type: SiteQuality
SIO_000300: 6.029e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.62e1

VQSLOD
type: SiteQuality
SIO_000300: 2.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.817e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3532
num of homozygotes: 0

African
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allele frequency: 1.434720229555237e-4
allele num: 6970
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East Asian
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allele count: 0
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European (Non-Finnish)
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allele count: 0
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Other
type: Population
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South Asian
type: Population
allele count: 1
allele frequency: 1.34661998384056e-4
allele num: 7426
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FS
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.257e0

MQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

DP
type: SiteQuality
SIO_000300: 1.426906e6

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

Latino
type: Population
allele count: 0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.533268778530917e-5
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East Asian
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South Asian
type: Population
allele count: 0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

DP
type: SiteQuality
SIO_000300: 1.412161e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.54e0

FS
type: SiteQuality
SIO_000300: 3.336e0

VQSLOD
type: SiteQuality
SIO_000300: -1.555e0

QD
type: SiteQuality
SIO_000300: 2.307e1

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

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

East Asian
type: Population
allele count: 6
allele frequency: 1.267962806424345e-3
allele num: 4732
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32439
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7010
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3210
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

QD
type: SiteQuality
SIO_000300: 1.48e1

VQSLOD
type: SiteQuality
SIO_000300: 5.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.55e-1

DP
type: SiteQuality
SIO_000300: 1.273492e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.782e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

European (Finnish)
type: Population
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allele frequency: 3.135779241141424e-4
allele num: 3189
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4677
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European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 7.483629560336763e-4
allele num: 32070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
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African
type: Population
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.73e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.26056e6

Other
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allele frequency: 0.0e0
allele num: 408
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 6278
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3136
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Latino
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allele frequency: 0.0e0
allele num: 5912
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East Asian
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allele count: 0
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DP
type: SiteQuality
SIO_000300: 1.228045e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.434e1

FS
type: SiteQuality
SIO_000300: 0.0e0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 30204
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 6765
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 395
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East Asian
type: Population
allele count: 3
allele frequency: 6.87442713107241e-4
allele num: 4364
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3059
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6129
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-2

FS
type: SiteQuality
SIO_000300: 1.312e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

QD
type: SiteQuality
SIO_000300: 2.416e1

DP
type: SiteQuality
SIO_000300: 1.180381e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.97e0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6579
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 375
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5900
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.538570417551309e-5
allele num: 28260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2943
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.87e-2

DP
type: SiteQuality
SIO_000300: 1.111323e6

VQSLOD
type: SiteQuality
SIO_000300: 2.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -9.27e-1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28052
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5148
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4012
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 5883
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2931
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Other
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allele frequency: 0.0e0
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.93e-2

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.019e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

FS
type: SiteQuality
SIO_000300: 1.0236e1

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Other
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2790
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25893
num of homozygotes: 0

Latino
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allele frequency: 4.339336081579518e-4
allele num: 4609
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.38e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

DP
type: SiteQuality
SIO_000300: 1.054501e6

QD
type: SiteQuality
SIO_000300: 1.359e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3600
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25668
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Latino
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 363
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2768
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South Asian
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MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.67e-2

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4156
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 24413
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2683
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South Asian
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Other
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.63e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

Other
type: Population
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allele frequency: 0.0e0
allele num: 157
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African
type: Population
allele count: 0
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East Asian
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allele frequency: 3.225806451612903e-3
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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South Asian
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DP
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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African
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allele frequency: 3.641660597232338e-4
allele num: 2746
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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FS
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
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BaseQRankSum
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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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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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European (Finnish)
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East Asian
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Latino
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African
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European (Non-Finnish)
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allele frequency: 1.965601965601966e-4
allele num: 10175
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Other
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-2

European (Non-Finnish)
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allele frequency: 3.368137420006736e-4
allele num: 11876
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European (Finnish)
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East Asian
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African
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Other
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South Asian
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 5.63226e5

European (Non-Finnish)
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East Asian
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Latino
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African
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South Asian
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Other
type: Population
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MQ
type: SiteQuality
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DP
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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European (Finnish)
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South Asian
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African
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Other
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East Asian
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European (Non-Finnish)
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.368e1

East Asian
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European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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African
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DP
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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South Asian
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African
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East Asian
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European (Non-Finnish)
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Other
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Latino
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QD
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ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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Other
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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DP
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ClippingRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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MQRankSum
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African
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East Asian
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Latino
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Other
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European (Finnish)
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InbreedingCoeff
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ClippingRankSum
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FS
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QD
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MQ
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MQRankSum
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DP
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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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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Other
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South Asian
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QD
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FS
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MQ
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InbreedingCoeff
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DP
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VQSLOD
type: SiteQuality
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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African
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Other
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DP
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MQRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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African
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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Other
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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Other
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South Asian
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VQSLOD
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MQ
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BaseQRankSum
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QD
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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South Asian
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Latino
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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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DP
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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QD
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FS
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MQ
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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Other
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Latino
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African
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East Asian
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European (Finnish)
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South Asian
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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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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African
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South Asian
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InbreedingCoeff
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MQ
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ReadPosRankSum
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BaseQRankSum
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FS
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DP
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QD
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VQSLOD
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MQRankSum
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ClippingRankSum
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South Asian
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Other
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African
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Latino
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East Asian
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European (Non-Finnish)
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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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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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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DP
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VQSLOD
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MQRankSum
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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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Latino
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Other
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DP
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MQ
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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Other
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African
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DP
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MQ
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BaseQRankSum
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ReadPosRankSum
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FS
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QD
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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South Asian
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Other
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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QD
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DP
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.99e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.601e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4281
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2839
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.417634996582365e-4
allele num: 2926
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4709
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18754
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 301
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.08865e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.77e0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.57e-2

QD
type: SiteQuality
SIO_000300: 1.221e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17903
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2018
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4142
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-2