http://identifiers.org/exac.variant/5-149824185-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149824185
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149824185
    reference: chr 5
allele count: 1
allele frequency: 8.773469029654326e-5
allele num: 11398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.*3G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.389-269G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.389-269G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.389-269G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.389-269G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3004-269G>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8856
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

5-149824191-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149824191
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149824191
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 11326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.389-275C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.389-275C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3004-275C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.402C>T
  hgvsp: ENST00000518139.1:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.389-275C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.389-275C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7978
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1241
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly134Gly
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

5-149824197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149824197
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149824197
    reference: chr 5
allele count: 1
allele frequency: 8.838607035531201e-5
allele num: 11314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.389-281G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3004-281G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.389-281G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.396G>A
  hgvsp: ENST00000518139.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.389-281G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.389-281G>A
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr132Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

5-149824209-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149824209
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149824209
    reference: chr 5
allele count: 2
allele frequency: 1.787629603146228e-4
allele num: 11188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.389-293T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.389-5T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.389-293T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.389-293T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3004-293T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.389-293T>C
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5783
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 2.25e1
  variant carriers: 0
hgvs: c.389-5T>C
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

5-149824223-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149824223
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149824223
    reference: chr 5
allele count: 3687
allele frequency: 3.306133428981349e-1
allele num: 11152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.389-307A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.389-19A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3004-307A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.389-307A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.389-307A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.389-307A>G
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 263
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.25e1
  variant carriers: 297
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 305
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 2.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 264
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 232
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 2.5e0
  variant carriers: 300
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 244
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 189
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.75e1
  variant carriers: 270
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 301
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 7.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 6.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 6.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 8.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 1.25e1
  variant carriers: 72
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.75e1
  variant carriers: 67
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 3200
  bin: 7.5e0
  variant carriers: 173
num of homozygotes: 652
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

5-149824983-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149824983
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149824983
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 15228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+189T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+189T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+189T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+189T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+189T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+189T>C
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36356
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26375
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2219
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2676
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3904
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7474
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

5-149824984-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149824984
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149824984
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 15216
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+188A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+188A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+188A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+188A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+188A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+188A>C
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36424
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3865
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4040
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2121
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7074
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26872
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

5-149824986-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149824986
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149824986
    reference: chr 5
allele count: 1
allele frequency: 6.56254101588135e-5
allele num: 15238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+186A>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+186A>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+186A>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+186A>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+186A>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+186A>T
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36547
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4042
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6440
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

5-149824991-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149824991
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149824991
    reference: chr 5
allele count: 1
allele frequency: 6.532532009406845e-5
allele num: 15308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.*32C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+181C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+181C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+181C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+181C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+181C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+181C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36787
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3443
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1599
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4809
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

5-149825007-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825007
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825007
    reference: chr 5
allele count: 240
allele frequency: 1.491795126802586e-2
allele num: 16088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+165C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+165C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+165C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+165C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+165C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+165C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 2.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 1.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12970
  bin: 7.5e0
  variant carriers: 313
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 34171
  bin: 2.5e0
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 1.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 8.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 8.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2419
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 7.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 10007
  bin: 2.25e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 6.25e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 9.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 30938
  bin: 7.5e0
  variant carriers: 29
num of homozygotes: 14
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

5-149825023-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825023
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825023
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 17810
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+149A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+149A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+149A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+149A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+149A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+149A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.362A>G
  hgvsp: ENSP00000428536.1:p.Ter121TrpextTer?
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: stop lost
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23380
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25910
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20545
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ter121TrpextTer?
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

5-149825024-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825024
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825024
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 18078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+148G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.361G>A
  hgvsp: ENST00000519855.1:c.361G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+148G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+148G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+148G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+148G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+148G>A
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: stop retained
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24376
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24929
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4050
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21512
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1613
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ter121Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

5-149825026-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825026
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825026
    reference: chr 5
allele count: 2
allele frequency: 1.075500107550011e-4
allele num: 18596
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+146G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+146G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.359G>A
  hgvsp: ENST00000519855.1:c.359G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+146G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+146G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+146G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+146G>A
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1694
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23695
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu120Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

5-149825031-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825031
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825031
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 20262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+141A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+141A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.354A>C
  hgvsp: ENSP00000428536.1:p.Thr119Pro
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+141A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+141A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+141A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+141A>C
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30166
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18515
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4052
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18007
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr119Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum

5-149825036-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825036
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825037
    reference: chr 5
allele count: 1
allele frequency: 4.283755997258396e-5
allele num: 23344
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+135dupA
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+135dupA
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+135dupA
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+135dupA
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.348dupA
  hgvsp: ENSP00000428536.1:p.Arg117LysfsTer7
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+135dupA
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+135dupA
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14817
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30889
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14405
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4054
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg117LysfsTer7
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

5-149825038-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825038
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825038
    reference: chr 5
allele count: 1
allele frequency: 4.127455836222553e-5
allele num: 24228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.347A>G
  hgvsp: ENST00000519855.1:c.347A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+134A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+134A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+134A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+134A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+134A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+134A>G
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13528
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3334
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2667
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13232
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32021
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1324
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala116Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

5-149825043-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825043
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825043
    reference: chr 5
allele count: 1
allele frequency: 3.544590954203885e-5
allele num: 28212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+129G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+129G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+129G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+129G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+129G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+129G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.342G>C
  hgvsp: ENSP00000428536.1:p.Ala115Pro
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4266
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10043
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9878
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33855
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala115Pro
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

5-149825046-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825046
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825046
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 30790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+126G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.339G>A
  hgvsp: ENSP00000428536.1:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+126G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+126G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+126G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+126G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+126G>A
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 36106
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34815
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4056
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1632
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu114Lys
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

5-149825050-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825050
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825050
    reference: chr 5
allele count: 1
allele frequency: 2.930832356389215e-5
allele num: 34120
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+122A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+122A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.335A>C
  hgvsp: ENSP00000428536.1:p.Leu112Phe
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+122A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+122A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+122A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+122A>C
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6705
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6655
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1826
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1822
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu112Phe
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

5-149825066-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825066
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825066
    reference: chr 5
allele count: 1
allele frequency: 1.932815338822529e-5
allele num: 51738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.319G>C
  hgvsp: ENSP00000428536.1:p.Trp107Ser
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+106G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+106G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+106G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+106G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+106G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+106G>C
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31658
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2065
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Trp107Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

5-149825067-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825067
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825067
    reference: chr 5
allele count: 1
allele frequency: 1.849386003846723e-5
allele num: 54072
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+105T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+105T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+105T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+105T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.318T>C
  hgvsp: ENSP00000428536.1:p.Trp107Arg
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+105T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+105T>C
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13359
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12818
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30885
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4055
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2035
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Trp107Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

5-149825068-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825068
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825068
    reference: chr 5
allele count: 1
allele frequency: 1.795396603109627e-5
allele num: 55698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+104T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+104T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+104T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+104T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+104T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.317T>C
  hgvsp: ENST00000519855.1:c.317T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+104T>C
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe106Phe
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

5-149825068-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825068
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825068
    reference: chr 5
allele count: 2
allele frequency: 3.590793206219254e-5
allele num: 55698
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+104T>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+104T>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+104T>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.317T>A
  hgvsp: ENSP00000428536.1:p.Phe106Leu
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+104T>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+104T>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+104T>A
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4057
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe106Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/5-149825075-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825075
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825075
    reference: chr 5
allele count: 1
allele frequency: 1.506795648374167e-5
allele num: 66366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.310G>T
  hgvsp: ENSP00000428536.1:p.Gly104Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+97G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+97G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+97G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+97G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+97G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+97G>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1779
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17696
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26074
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly104Val
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/5-149825077-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825077
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825077
    reference: chr 5
allele count: 1
allele frequency: 1.395946172315595e-5
allele num: 71636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+95T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+95T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+95T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+95T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+95T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.308T>G
  hgvsp: ENST00000519855.1:c.308T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+95T>G
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24055
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1873
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser103Ser
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/5-149825079-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825079
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825079
    reference: chr 5
allele count: 1
allele frequency: 1.340590396010403e-5
allele num: 74594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+93T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+93T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+93T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+93T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.306T>G
  hgvsp: ENSP00000428536.1:p.Ser103Ala
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+93T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+93T>G
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 22558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22472
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4044
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1829
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 2.75e1
  variant carriers: 1
hgvs: p.Ser103Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/5-149825084-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825084
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825084
    reference: chr 5
allele count: 1
allele frequency: 1.180080245456691e-5
allele num: 84740
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+88G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.301G>T
  hgvsp: ENSP00000428536.1:p.Gly101Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+88G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+88G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+88G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+88G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+88G>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27200
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18068
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4065
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1956
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly101Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

5-149825084-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825084
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825084
    reference: chr 5
allele count: 1
allele frequency: 1.180080245456691e-5
allele num: 84740
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+88G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.301G>C
  hgvsp: ENSP00000428536.1:p.Gly101Ala
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+88G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+88G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+88G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+88G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+88G>C
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18068
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27192
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1956
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly101Ala
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD

5-149825086-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825086
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825086
    reference: chr 5
allele count: 1
allele frequency: 1.100497424836026e-5
allele num: 90868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+86C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+86C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+86C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.299C>T
  hgvsp: ENST00000519855.1:c.299C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+86C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+86C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+86C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14663
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1216
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15167
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2204
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4071
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser100Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

5-149825094-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825094
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825094
    reference: chr 5
allele count: 1
allele frequency: 9.714019272614236e-6
allele num: 102944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+78A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.291A>G
  hgvsp: ENSP00000428536.1:p.Met98Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+78A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+78A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+78A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+78A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+78A>G
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9421
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4078
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2559
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37332
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Met98Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/5-149825105-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825105
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825105
    reference: chr 5
allele count: 3
allele frequency: 2.686775690053556e-5
allele num: 111658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+67G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+67G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+67G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.280G>T
  hgvsp: ENSP00000428536.1:p.Cys94Phe
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+67G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+67G>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+67G>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39072
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7902
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5082
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys94Phe
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

5-149825106-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825106
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825106
    reference: chr 5
allele count: 5
allele frequency: 4.44026073211019e-5
allele num: 112606
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+66T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+66T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.279T>C
  hgvsp: ENSP00000428536.1:p.Cys94Arg
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+66T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+66T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+66T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+66T>C
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8031
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39609
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3025
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4612
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Cys94Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

5-149825110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825110
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825110
    reference: chr 5
allele count: 5
allele frequency: 4.350777048780912e-5
allele num: 114922
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+62G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+62G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.275G>A
  hgvsp: ENST00000519855.1:c.275G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+62G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+62G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+62G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+62G>A
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3090
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4101
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr92Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

5-149825111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825111
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825111
    reference: chr 5
allele count: 30
allele frequency: 2.595380223202699e-4
allele num: 115590
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+61C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+61C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+61C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.274C>T
  hgvsp: ENSP00000428536.1:p.Thr92Met
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+61C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+61C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+61C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40606
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8812
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3081
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr92Met
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

5-149825111-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825111
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825111
    reference: chr 5
allele count: 2
allele frequency: 1.730253482135133e-5
allele num: 115590
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+61C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+61C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.274C>G
  hgvsp: ENSP00000428536.1:p.Thr92Arg
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+61C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+61C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+61C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+61C>G
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3133
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr92Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

5-149825117-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825117
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825117
    reference: chr 5
allele count: 1
allele frequency: 8.51397142711189e-6
allele num: 117454
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+55A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.268A>C
  hgvsp: ENSP00000428536.1:p.Lys90Thr
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+55A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+55A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+55A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+55A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+55A>C
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9514
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3269
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4112
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys90Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum

5-149825118-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825118
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825118
    reference: chr 5
allele count: 1918
allele frequency: 1.628515147398451e-2
allele num: 117776
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+54A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+54A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+54A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.267A>G
  hgvsp: ENSP00000428536.1:p.Lys90Glu
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+54A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+54A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+54A>G
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.75e1
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 40183
  bin: 2.25e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 9493
  bin: 2.75e1
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 3.25e1
  variant carriers: 242
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.75e1
  variant carriers: 254
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.25e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 5.25e1
  variant carriers: 128
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 8.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 8.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 45435
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 5.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3083
  bin: 6.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys90Glu
num of homozygotes: 104
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

5-149825128-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825128
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825128
    reference: chr 5
allele count: 2
allele frequency: 1.674116485025028e-5
allele num: 119466
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+44A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+44A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+44A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.257A>G
  hgvsp: ENST00000519855.1:c.257A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+44A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+44A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+44A>G
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3359
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4250
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala86Ala
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

5-149825129-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825129
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825129
    reference: chr 5
allele count: 922
allele frequency: 7.704134496473812e-3
allele num: 119676
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+43C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+43C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+43C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+43C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.256C>T
  hgvsp: ENSP00000428536.1:p.Ala86Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+43C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+43C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 39985
  bin: 2.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 6.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 3.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 2.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47530
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala86Val
num of homozygotes: 35
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/5-149825145-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825145
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825145
    reference: chr 5
allele count: 1
allele frequency: 8.29393713195654e-6
allele num: 120570
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+27T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.240T>G
  hgvsp: ENSP00000428536.1:p.Trp81Gly
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+27T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+27T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+27T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+27T>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+27T>G
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Trp81Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

5-149825158-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825158
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825159
    reference: chr 5
allele count: 1
allele frequency: 8.277049397430804e-6
allele num: 120816
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+13dupC
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.226dupC
  hgvsp: ENSP00000428536.1:p.Leu77SerfsTer3
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+13dupC
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+13dupC
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+13dupC
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+13dupC
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+13dupC
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4224
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu77SerfsTer3
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

5-149825159-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825159
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825159
    reference: chr 5
allele count: 9
allele frequency: 7.447988215627534e-5
allele num: 120838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+13C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.226C>T
  hgvsp: ENSP00000428536.1:p.Pro76Leu
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+13C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+13C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+13C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+13C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+13C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro76Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

5-149825159-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825159
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825159
    reference: chr 5
allele count: 5348
allele frequency: 4.425760108575117e-2
allele num: 120838
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+13C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+13C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+13C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+13C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+13C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+13C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.226C>G
  hgvsp: ENSP00000428536.1:p.Pro76Arg
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 11392
  bin: 2.75e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 275
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 358
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 400
genotype depth: GenotypeDepth
  all individuals: 37844
  bin: 2.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.25e1
  variant carriers: 580
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.25e1
  variant carriers: 493
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 5.75e1
  variant carriers: 581
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 4.25e1
  variant carriers: 482
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 185
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 186
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 3.25e1
  variant carriers: 188
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 609
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 2979
  bin: 6.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 7.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46710
  bin: 6.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 3
hgvs: p.Pro76Arg
num of homozygotes: 570
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

5-149825161-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825161
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825161
    reference: chr 5
allele count: 1
allele frequency: 8.27348843366317e-6
allele num: 120868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+11C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+11C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+11C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+11C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.224C>G
  hgvsp: ENST00000519855.1:c.224C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+11C>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+11C>G
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3455
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4258
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro75Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

5-149825163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825163
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825163
    reference: chr 5
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+9C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.222C>T
  hgvsp: ENSP00000428536.1:p.Pro75Ser
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+9C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+9C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+9C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+9C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+9C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro75Ser
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

5-149825163-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825163
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825163
    reference: chr 5
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.222C>A
  hgvsp: ENSP00000428536.1:p.Pro75Thr
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.388+9C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.3003+9C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.388+9C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.388+9C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.388+9C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.388+9C>A
  variant of: http://identifiers.org/hgnc/10387
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4259
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro75Thr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum

5-149825177-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825177
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825177
    reference: chr 5
allele count: 1
allele frequency: 8.269383434771103e-6
allele num: 120928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.383G>A
  hgvsp: ENSP00000429856.1:p.Arg128Gln
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.208G>A
  hgvsp: ENSP00000428536.1:p.Arg70Gln
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.383G>A
  hgvsp: ENSP00000385425.1:p.Arg128Gln
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.383G>A
  hgvsp: ENSP00000311028.5:p.Arg128Gln
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.383G>A
  hgvsp: ENSP00000428509.1:p.Arg128Gln
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2998G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.383G>A
  hgvsp: ENSP00000385958.3:p.Arg128Gln
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13546
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3442
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg128Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

5-149825182-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825182
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825182
    reference: chr 5
allele count: 2
allele frequency: 1.65371258475277e-5
allele num: 120940
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.378C>T
  hgvsp: ENST00000401695.3:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.378C>T
  hgvsp: ENST00000407193.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.378C>T
  hgvsp: ENST00000312037.5:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.203C>T
  hgvsp: ENST00000519855.1:c.203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.378C>T
  hgvsp: ENST00000521466.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2993C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.378C>T
  hgvsp: ENST00000518139.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile126Ile
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD

5-149825184-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825184
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825184
    reference: chr 5
allele count: 1
allele frequency: 8.269383434771103e-6
allele num: 120928
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.376A>G
  hgvsp: ENSP00000311028.5:p.Ile126Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.376A>G
  hgvsp: ENSP00000428509.1:p.Ile126Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.376A>G
  hgvsp: ENSP00000429856.1:p.Ile126Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.201A>G
  hgvsp: ENSP00000428536.1:p.Ile68Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.376A>G
  hgvsp: ENSP00000385425.1:p.Ile126Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.376A>G
  hgvsp: ENSP00000385958.3:p.Ile126Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2991A>G
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13585
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49702
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile126Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

5-149825185-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825185
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825185
    reference: chr 5
allele count: 1
allele frequency: 8.270614506657845e-6
allele num: 120910
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.375G>A
  hgvsp: ENST00000407193.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.200G>A
  hgvsp: ENST00000519855.1:c.200G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.375G>A
  hgvsp: ENST00000521466.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2990G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.375G>A
  hgvsp: ENST00000518139.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.375G>A
  hgvsp: ENST00000401695.3:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.375G>A
  hgvsp: ENST00000312037.5:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49617
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3460
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys125Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

5-149825190-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825190
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825190
    reference: chr 5
allele count: 1
allele frequency: 8.273077750384698e-6
allele num: 120874
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.370A>G
  hgvsp: ENSP00000311028.5:p.Met124Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.370A>G
  hgvsp: ENSP00000385958.3:p.Met124Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.370A>G
  hgvsp: ENSP00000429856.1:p.Met124Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2985A>G
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.370A>G
  hgvsp: ENSP00000385425.1:p.Met124Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.195A>G
  hgvsp: ENSP00000428536.1:p.Met66Val
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.370A>G
  hgvsp: ENSP00000428509.1:p.Met124Val
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49478
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Met124Val
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

5-149825193-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825193
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825193
    reference: chr 5
allele count: 2
allele frequency: 1.654861984510492e-5
allele num: 120856
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.367G>A
  hgvsp: ENSP00000385958.3:p.Gly123Ser
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.367G>A
  hgvsp: ENSP00000429856.1:p.Gly123Ser
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.367G>A
  hgvsp: ENSP00000385425.1:p.Gly123Ser
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.367G>A
  hgvsp: ENSP00000428509.1:p.Gly123Ser
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2982G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.192G>A
  hgvsp: ENSP00000428536.1:p.Gly65Ser
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.367G>A
  hgvsp: ENSP00000311028.5:p.Gly123Ser
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4253
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49426
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly123Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

5-149825194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825194
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825194
    reference: chr 5
allele count: 4
allele frequency: 3.310107412985551e-5
allele num: 120842
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.366G>A
  hgvsp: ENST00000518139.1:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.366G>A
  hgvsp: ENST00000312037.5:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.191G>A
  hgvsp: ENST00000519855.1:c.191G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2981G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.366G>A
  hgvsp: ENST00000401695.3:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.366G>A
  hgvsp: ENST00000521466.1:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.366G>A
  hgvsp: ENST00000407193.1:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4257
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser122Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

5-149825198-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825198
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825198
    reference: chr 5
allele count: 1
allele frequency: 8.277460475126231e-6
allele num: 120810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.362G>A
  hgvsp: ENSP00000428509.1:p.Arg121His
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.362G>A
  hgvsp: ENSP00000429856.1:p.Arg121His
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.362G>A
  hgvsp: ENSP00000385425.1:p.Arg121His
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2977G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.362G>A
  hgvsp: ENSP00000311028.5:p.Arg121His
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.187G>A
  hgvsp: ENSP00000428536.1:p.Arg63His
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.362G>A
  hgvsp: ENSP00000385958.3:p.Arg121His
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49353
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg121His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

5-149825200-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825200
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825200
    reference: chr 5
allele count: 2
allele frequency: 1.655519502019734e-5
allele num: 120808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.360C>T
  hgvsp: ENST00000312037.5:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.360C>T
  hgvsp: ENST00000521466.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.360C>T
  hgvsp: ENST00000407193.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2975C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.185C>T
  hgvsp: ENST00000519855.1:c.185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.360C>T
  hgvsp: ENST00000401695.3:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.360C>T
  hgvsp: ENST00000518139.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49494
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala120Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

5-149825218-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825218
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825218
    reference: chr 5
allele count: 1
allele frequency: 8.301648707433296e-6
allele num: 120458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.342G>A
  hgvsp: ENST00000518139.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2957G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.342G>A
  hgvsp: ENST00000407193.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.342G>A
  hgvsp: ENST00000521466.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.342G>A
  hgvsp: ENST00000312037.5:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.167G>A
  hgvsp: ENST00000519855.1:c.167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.342G>A
  hgvsp: ENST00000401695.3:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48863
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4254
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser114Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

5-149825219-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825219
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825219
    reference: chr 5
allele count: 4
allele frequency: 3.320824892903397e-5
allele num: 120452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.166C>T
  hgvsp: ENSP00000428536.1:p.Ser56Leu
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.341C>T
  hgvsp: ENSP00000385425.1:p.Ser114Leu
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.341C>T
  hgvsp: ENSP00000428509.1:p.Ser114Leu
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.341C>T
  hgvsp: ENSP00000429856.1:p.Ser114Leu
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.341C>T
  hgvsp: ENSP00000385958.3:p.Ser114Leu
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2956C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.341C>T
  hgvsp: ENSP00000311028.5:p.Ser114Leu
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49014
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser114Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

5-149825227-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825227
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825227
    reference: chr 5
allele count: 1
allele frequency: 8.327226700419692e-6
allele num: 120088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.333G>A
  hgvsp: ENST00000407193.1:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.333G>A
  hgvsp: ENST00000518139.1:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.333G>A
  hgvsp: ENST00000521466.1:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2948G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.333G>A
  hgvsp: ENST00000312037.5:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.158G>A
  hgvsp: ENST00000519855.1:c.158G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.333G>A
  hgvsp: ENST00000401695.3:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly111Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

5-149825238-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825238
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825238
    reference: chr 5
allele count: 1
allele frequency: 8.375349670848758e-6
allele num: 119398
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.322C>A
  hgvsp: ENSP00000385958.3:p.Pro108Thr
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.147C>A
  hgvsp: ENSP00000428536.1:p.Pro50Thr
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2937C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.322C>A
  hgvsp: ENSP00000311028.5:p.Pro108Thr
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.322C>A
  hgvsp: ENSP00000428509.1:p.Pro108Thr
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.322C>A
  hgvsp: ENSP00000385425.1:p.Pro108Thr
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.322C>A
  hgvsp: ENSP00000429856.1:p.Pro108Thr
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1819
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3228
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4247
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro108Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

5-149825239-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825239
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825239
    reference: chr 5
allele count: 21
allele frequency: 1.760091189486389e-4
allele num: 119312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.321C>T
  hgvsp: ENST00000312037.5:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.146C>T
  hgvsp: ENST00000519855.1:c.146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.321C>T
  hgvsp: ENST00000521466.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.321C>T
  hgvsp: ENST00000518139.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.321C>T
  hgvsp: ENST00000401695.3:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.321C>T
  hgvsp: ENST00000407193.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2936C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13227
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47696
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr107Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

5-149825262-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825262
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825262
    reference: chr 5
allele count: 3
allele frequency: 2.622606871230003e-5
allele num: 114390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.312-14C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.312-14C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.137-14C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.312-14C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.312-14C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.312-14C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2927-14C>A
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11121
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38510
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7345
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ

5-149825263-T-TAAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825263
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825267
    reference: chr 5
allele count: 1
allele frequency: 8.756567425569177e-6
allele num: 114200
alternate allele: TAAAA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.312-16_312-15insTTTT
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.312-16_312-15insTTTT
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.137-16_137-15insTTTT
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.312-16_312-15insTTTT
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2927-16_2927-15insTTTT
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.312-16_312-15insTTTT
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.312-16_312-15insTTTT
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10876
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

5-149825273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825273
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825273
    reference: chr 5
allele count: 1
allele frequency: 8.960091751339533e-6
allele num: 111606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.312-25C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2927-25C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.312-25C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.312-25C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.312-25C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.312-25C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.137-25C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27870
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10778
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4643
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS

5-149825276-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825276
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825276
    reference: chr 5
allele count: 1
allele frequency: 9.013718880135566e-6
allele num: 110942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.312-28C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.312-28C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.312-28C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.312-28C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.137-28C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.312-28C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2927-28C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19629
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4247
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

5-149825279-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825279
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825279
    reference: chr 5
allele count: 4
allele frequency: 3.630554748765611e-5
allele num: 110176
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.312-31G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.312-31G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.312-31G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.312-31G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.312-31G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2927-31G>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.137-31G>C
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8283
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17566
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4260
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4384
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6591
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-149825287-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825287
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825287
    reference: chr 5
allele count: 1
allele frequency: 9.284533823556719e-6
allele num: 107706
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.312-39G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.312-39G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.312-39G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.312-39G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.137-39G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2927-39G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.312-39G>A
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12016
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8170
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2522
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

5-149825297-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825297
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825297
    reference: chr 5
allele count: 1
allele frequency: 9.616679168349585e-6
allele num: 103986
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.312-49C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.137-49C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.312-49C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.312-49C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2927-49C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.312-49C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.312-49C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6941
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4810
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3224
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8381
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9429
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7331
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4248
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP

5-149825299-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825299
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825299
    reference: chr 5
allele count: 553
allele frequency: 5.348265923905685e-3
allele num: 103398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.312-51T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.137-51T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.312-51T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.312-51T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.312-51T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.312-51T>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2927-51T>C
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16034
  bin: 1.25e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 15490
  bin: 1.75e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7112
  bin: 7.5e0
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 2.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 11876
  bin: 2.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1263
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6080
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1542
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3092
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 9.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 8369
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.75e1
  variant carriers: 13
num of homozygotes: 9
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ

5-149825300-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149825300
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149825300
    reference: chr 5
allele count: 1
allele frequency: 9.742031018626763e-6
allele num: 102648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.312-52C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.312-52C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2927-52C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.312-52C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.312-52C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.137-52C>T
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.312-52C>T
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16035
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8401
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4830
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5379
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1535
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4286
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3280
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

5-149826314-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149826314
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149826314
    reference: chr 5
allele count: 1
allele frequency: 8.532132009146445e-6
allele num: 117204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2926+51G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.136+51G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.311+51G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.311+51G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.311+51G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.311+51G>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.311+51G>A
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7390
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7594
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

5-149826326-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149826326
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149826326
    reference: chr 5
allele count: 3
allele frequency: 2.554800470083287e-5
allele num: 117426
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.311+39C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2926+39C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.311+39C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.311+39C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.136+39C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.311+39C>A
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.311+39C>A
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7611
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3140
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1977
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2304
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

5-149826351-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 149826351
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 149826351
    reference: chr 5
allele count: 1
allele frequency: 8.404067568703253e-6
allele num: 118990
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385958
  ensembl transcript: ENST00000401695
  gene symbol: RPS14
  hgvsc: ENST00000401695.3:c.311+14A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl transcript: ENST00000519690
  gene symbol: RPS14
  hgvsc: ENST00000519690.1:n.2926+14A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000429856
  ensembl transcript: ENST00000518139
  gene symbol: RPS14
  hgvsc: ENST00000518139.1:c.311+14A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000311028
  ensembl transcript: ENST00000312037
  gene symbol: RPS14
  hgvsc: ENST00000312037.5:c.311+14A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428509
  ensembl transcript: ENST00000521466
  gene symbol: RPS14
  hgvsc: ENST00000521466.1:c.311+14A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000385425
  ensembl transcript: ENST00000407193
  gene symbol: RPS14
  hgvsc: ENST00000407193.1:c.311+14A>C
  variant of: http://identifiers.org/hgnc/10387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164587
  ensembl protein: ENSP00000428536
  ensembl transcript: ENST00000519855
  gene symbol: RPS14
  hgvsc: ENST00000519855.1:c.136+14A>C
  variant of: http://identifiers.org/hgnc/10387
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2046
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 509
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2044
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7949
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.330140994945464e-4
allele num: 7518
num of homozygotes: 0

African
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: 3192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.856e0

VQSLOD
type: SiteQuality
SIO_000300: -1.119e0

FS
type: SiteQuality
SIO_000300: 2.597e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.67e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.69e-1

QD
type: SiteQuality
SIO_000300: 1.52e1

MQ
type: SiteQuality
SIO_000300: 5.909e1

DP
type: SiteQuality
SIO_000300: 2.16529e5

ClippingRankSum
type: SiteQuality
SIO_000300: 6.69e-1

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

GenotypeQuality
all individuals: 6855
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.067e0

DP
type: SiteQuality
SIO_000300: 2.1396e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.560000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.18e0

QD
type: SiteQuality
SIO_000300: 1.239e1

GenotypeQuality
all individuals: 145
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6512
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2047
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 322
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.330849081714134e-4
allele num: 7514
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.11766e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.35e-2

FS
type: SiteQuality
SIO_000300: 1.1839e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.4e-1

QD
type: SiteQuality
SIO_000300: 6.7e0

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.662406815761449e-4
allele num: 7512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 5.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.14e-2

MQ
type: SiteQuality
SIO_000300: 5.908e1

VQSLOD
type: SiteQuality
SIO_000300: 4.1e-2

QD
type: SiteQuality
SIO_000300: 8.84e0

DP
type: SiteQuality
SIO_000300: 2.08941e5

ClippingRankSum
type: SiteQuality
SIO_000300: 6.45e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 6

GenotypeQuality
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bin: 5.25e1
variant carriers: 17

GenotypeQuality
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bin: 2.5e0
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 40

GenotypeQuality
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bin: 5.75e1
variant carriers: 19

GenotypeQuality
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variant carriers: 3024

GenotypeQuality
all individuals: 230
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GenotypeQuality
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variant carriers: 13

Other
type: Population
allele count: 42
allele frequency: 3.333333333333333e-1
allele num: 126
num of homozygotes: 5

South Asian
type: Population
allele count: 2914
allele frequency: 3.882227551292299e-1
allele num: 7506
num of homozygotes: 568

East Asian
type: Population
allele count: 35
allele frequency: 2.5e-1
allele num: 140
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 629
allele frequency: 2.060943643512451e-1
allele num: 3052
num of homozygotes: 67

African
type: Population
allele count: 32
allele frequency: 1.415929203539823e-1
allele num: 226
num of homozygotes: 3

Latino
type: Population
allele count: 35
allele frequency: 3.431372549019608e-1
allele num: 102
num of homozygotes: 6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

DP
type: SiteQuality
SIO_000300: 3.07693e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.054e-1

FS
type: SiteQuality
SIO_000300: 1.143e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

QD
type: SiteQuality
SIO_000300: 1.581e1

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 217
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variant carriers: 0

GenotypeQuality
all individuals: 4040
bin: 9.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7876
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 50
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1098
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5334
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.921e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

QD
type: SiteQuality
SIO_000300: 7.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.42188e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.74e-2

GenotypeQuality
all individuals: 185
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2836
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
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variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
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variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1098
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7876
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 4.43416e5

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.679999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.607e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 27687
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3810
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 1962
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variant carriers: 0

GenotypeQuality
all individuals: 181
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GenotypeQuality
all individuals: 272
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.871958068139274e-4
allele num: 5342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1104
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7874
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.01e0

DP
type: SiteQuality
SIO_000300: 4.45689e5

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.59e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.295e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 222
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 272
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variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1104
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.849796522382538e-4
allele num: 5406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.54245e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.22e0

VQSLOD
type: SiteQuality
SIO_000300: -3.099e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.033e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.35e-2

GenotypeQuality
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bin: 5.75e1
variant carriers: 18

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 41

GenotypeQuality
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variant carriers: 35

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4305
bin: 9.75e1
variant carriers: 291

GenotypeQuality
all individuals: 259
bin: 7.75e1
variant carriers: 9

Latino
type: Population
allele count: 9
allele frequency: 2.472527472527472e-2
allele num: 364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.952380952380952e-3
allele num: 168
num of homozygotes: 0

African
type: Population
allele count: 228
allele frequency: 1.745788667687596e-1
allele num: 1306
num of homozygotes: 14

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
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South Asian
type: Population
allele count: 1
allele frequency: 1.262945188178833e-4
allele num: 7918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.720578114246387e-4
allele num: 5812
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.0344e5

QD
type: SiteQuality
SIO_000300: 1.41e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

FS
type: SiteQuality
SIO_000300: 2.891e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.134e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

Latino
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: 6908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 228
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8032
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1500
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-2

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

DP
type: SiteQuality
SIO_000300: 5.74836e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.706e0

GenotypeQuality
all individuals: 1849
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 246
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East Asian
type: Population
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allele frequency: 0.0e0
allele num: 544
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African
type: Population
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allele frequency: 0.0e0
allele num: 1534
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Latino
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 7068
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.51e-1

FS
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.75e-2

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.82657e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4051
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variant carriers: 2

GenotypeQuality
all individuals: 247
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.705627705627706e-4
allele num: 7392
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8088
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

VQSLOD
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
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SIO_000300: 1.988e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.381e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.42e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.96429e5

QD
type: SiteQuality
SIO_000300: 1.483e1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 444
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1708
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

East 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: 208
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.82e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.772e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.33571e5

QD
type: SiteQuality
SIO_000300: 6.5e0

MQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 9.569377990430622e-5
allele num: 10450
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1926
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 6.098e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.05e-2

DP
type: SiteQuality
SIO_000300: 6.68185e5

VQSLOD
type: SiteQuality
SIO_000300: 5.13e0

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 942
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2006
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 9.038322487346348e-5
allele num: 11064
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.81e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -8.579e-1

FS
type: SiteQuality
SIO_000300: 6.892e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.31e-1

DP
type: SiteQuality
SIO_000300: 6.80719e5

QD
type: SiteQuality
SIO_000300: 7.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8748
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 8.431703204047217e-4
allele num: 1186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 986
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 13694
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1018
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.27e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.932e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.137e1

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 7.21272e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.749e0

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1206
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1190
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 15358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8912
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-2

ClippingRankSum
type: SiteQuality
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MQ
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DP
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 4.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 5.737893045673629e-5
allele num: 17428
num of homozygotes: 0

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

ReadPosRankSum
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MQ
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MQRankSum
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FS
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InbreedingCoeff
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DP
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VQSLOD
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QD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -4.49e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 4094
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 28916
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 2524
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Other
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South Asian
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East Asian
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allele frequency: 3.725782414307004e-4
allele num: 2684
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 2724
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.25684e5

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

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

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

Latino
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East Asian
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allele frequency: 3.528581510232887e-4
allele num: 2834
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

African
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allele frequency: 2.28310502283105e-4
allele num: 4380
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Other
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East Asian
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allele frequency: 0.0e0
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10716
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.207184092366902e-4
allele num: 3118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2706
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.28310502283105e-4
allele num: 4380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2932
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.32e-1

DP
type: SiteQuality
SIO_000300: 9.5586e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.061e1

GenotypeQuality
all individuals: 1213
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4290
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37874
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.928268414963363e-4
allele num: 5186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3266
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3694
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

DP
type: SiteQuality
SIO_000300: 1.041747e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.147e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

QD
type: SiteQuality
SIO_000300: 1.688e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20903
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5630
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.326394671107411e-5
allele num: 12010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4970
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4092
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.764999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.94e-1

DP
type: SiteQuality
SIO_000300: 1.083155e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

QD
type: SiteQuality
SIO_000300: 8.02e0

GenotypeQuality
all individuals: 235
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 312
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variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.713502398903359e-4
allele num: 5836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

MQ
type: SiteQuality
SIO_000300: 5.927e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

FS
type: SiteQuality
SIO_000300: 3.07626e2

VQSLOD
type: SiteQuality
SIO_000300: -4.353e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.588e0

QD
type: SiteQuality
SIO_000300: 2.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.318e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e0

DP
type: SiteQuality
SIO_000300: 1.110998e6

GenotypeQuality
all individuals: 1082
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1387
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
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variant carriers: 0

GenotypeQuality
all individuals: 468
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variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.938735944164405e-4
allele num: 5158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48074
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6780
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4216
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.511e1

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

DP
type: SiteQuality
SIO_000300: 1.194256e6

GenotypeQuality
all individuals: 669
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
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variant carriers: 0

GenotypeQuality
all individuals: 437
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variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
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variant carriers: 0

GenotypeQuality
all individuals: 4065
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1082
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48074
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13128
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.474926253687316e-4
allele num: 6780
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.194256e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.511e1

GenotypeQuality
all individuals: 1429
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30883
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 427
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 404
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variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.741553465691397e-4
allele num: 5742
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13636
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.34e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.2493e6

GenotypeQuality
all individuals: 855
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 986
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variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6824
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.736412571627019e-5
allele num: 57590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8222
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14790
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.569e0

QD
type: SiteQuality
SIO_000300: 1.706e1

FS
type: SiteQuality
SIO_000300: 4.74e0

DP
type: SiteQuality
SIO_000300: 1.352585e6

MQRankSum
type: SiteQuality
SIO_000300: -8.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.935e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.588e0

GenotypeQuality
all individuals: 506
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 42543
bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4087
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 451
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2952
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9004
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15572
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.803214352457484e-4
allele num: 10702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5818
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.243e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.69e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.440526e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.31e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 803
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 373
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GenotypeQuality
all individuals: 273
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GenotypeQuality
all individuals: 538
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variant carriers: 0

GenotypeQuality
all individuals: 4092
bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.405944716697095e-5
allele num: 62442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5870
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.257544899092761e-5
allele num: 10802
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.679e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

DP
type: SiteQuality
SIO_000300: 1.449069e6

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

QD
type: SiteQuality
SIO_000300: 1.279e1

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 836
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3425
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44724
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.145002145002145e-4
allele num: 9324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.144851877476571e-5
allele num: 63596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.284565108094519e-5
allele num: 15912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6050
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.474466e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.313e0

QD
type: SiteQuality
SIO_000300: 1.336e1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 7.276e0

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

GenotypeQuality
all individuals: 3133
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 290
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 45108
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4125
bin: 9.75e1
variant carriers: 28

GenotypeQuality
all individuals: 810
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 26
allele frequency: 2.768313458262351e-3
allele num: 9392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.249843769528809e-4
allele num: 16002
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.221001221001221e-4
allele num: 8190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564259792266299e-5
allele num: 63928
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11130
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.482405e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.302e1

MQ
type: SiteQuality
SIO_000300: 5.964e1

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

GenotypeQuality
all individuals: 326
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4125
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3081
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.249843769528809e-4
allele num: 16002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63928
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11130
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.34e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.482405e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

QD
type: SiteQuality
SIO_000300: 1.302e1

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 252
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46591
bin: 6.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543733983759918e-5
allele num: 64778
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8412
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.854e0

MQRankSum
type: SiteQuality
SIO_000300: -8.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.563e-1

DP
type: SiteQuality
SIO_000300: 1.503686e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.755e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e0

GenotypeQuality
all individuals: 195
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 300
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 375
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 812
bin: 7.75e1
variant carriers: 12

GenotypeQuality
all individuals: 5759
bin: 9.75e1
variant carriers: 1756

GenotypeQuality
all individuals: 190
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 350
allele frequency: 5.396903719237648e-3
allele num: 64852
num of homozygotes: 2

Latino
type: Population
allele count: 99
allele frequency: 8.731698712294938e-3
allele num: 11338
num of homozygotes: 1

Other
type: Population
allele count: 11
allele frequency: 1.273148148148148e-2
allele num: 864
num of homozygotes: 0

African
type: Population
allele count: 1408
allele frequency: 1.437614866244639e-1
allele num: 9794
num of homozygotes: 100

European (Finnish)
type: Population
allele count: 44
allele frequency: 6.97084917617237e-3
allele num: 6312
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.706907203756332e-4
allele num: 16186
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.08e-2

DP
type: SiteQuality
SIO_000300: 1.537088e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e0

QD
type: SiteQuality
SIO_000300: 1.608e1

VQSLOD
type: SiteQuality
SIO_000300: 6.87e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.04e-1

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

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47932
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522023682688503e-5
allele num: 65702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.1441647597254e-3
allele num: 874
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.68e1

FS
type: SiteQuality
SIO_000300: 1.2779e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.94e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.599e0

DP
type: SiteQuality
SIO_000300: 1.537563e6

GenotypeQuality
all individuals: 172
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3266
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5036
bin: 9.75e1
variant carriers: 879

GenotypeQuality
all individuals: 379
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 166
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 827
bin: 7.75e1
variant carriers: 2

African
type: Population
allele count: 846
allele frequency: 8.392857142857142e-2
allele num: 10080
num of homozygotes: 35

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.694760820045558e-3
allele num: 878
num of homozygotes: 0

Latino
type: Population
allele count: 57
allele frequency: 4.966887417218543e-3
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.128565346956152e-4
allele num: 65772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.63e-2

MQ
type: SiteQuality
SIO_000300: 5.978e1

VQSLOD
type: SiteQuality
SIO_000300: 4.78e0

QD
type: SiteQuality
SIO_000300: 1.403e1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

FS
type: SiteQuality
SIO_000300: 6.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.844e0

DP
type: SiteQuality
SIO_000300: 1.558518e6

GenotypeQuality
all individuals: 3452
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49095
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4220
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509479531457553e-5
allele num: 66248
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.95e-1

DP
type: SiteQuality
SIO_000300: 1.55445e6

FS
type: SiteQuality
SIO_000300: 5.388e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.331e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.38e-1

QD
type: SiteQuality
SIO_000300: 9.699999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.44e-1

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 1

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

GenotypeQuality
all individuals: 49281
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
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variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3471
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.771350400625366e-5
allele num: 10234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66410
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.225e0

QD
type: SiteQuality
SIO_000300: 6.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.399999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 4.357e0

DP
type: SiteQuality
SIO_000300: 1.558731e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

GenotypeQuality
all individuals: 369
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46710
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8063
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 9
allele frequency: 8.782201405152225e-4
allele num: 10248
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.528e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

DP
type: SiteQuality
SIO_000300: 1.687869e6

FS
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.473e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.811e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 295
bin: 9.25e1
variant carriers: 19

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 10

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 369
bin: 8.25e1
variant carriers: 9

GenotypeQuality
all individuals: 342
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 7

GenotypeQuality
all individuals: 604
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 8063
bin: 9.75e1
variant carriers: 4679

Other
type: Population
allele count: 29
allele frequency: 3.236607142857143e-2
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 144
allele frequency: 2.168282840450521e-3
allele num: 66412
num of homozygotes: 1

East Asian
type: Population
allele count: 2643
allele frequency: 3.063992580570369e-1
allele num: 8626
num of homozygotes: 390

African
type: Population
allele count: 292
allele frequency: 2.849336455893833e-2
allele num: 10248
num of homozygotes: 6

Latino
type: Population
allele count: 54
allele frequency: 4.672088596643018e-3
allele num: 11558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

South Asian
type: Population
allele count: 2186
allele frequency: 1.324848484848485e-1
allele num: 16500
num of homozygotes: 173

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

FS
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

DP
type: SiteQuality
SIO_000300: 1.687869e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.811e-1

QD
type: SiteQuality
SIO_000300: 1.473e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.528e0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49771
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 335
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.765625000000001e-5
allele num: 10240
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.3e-1

DP
type: SiteQuality
SIO_000300: 1.573817e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.115e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.28e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.046e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.716e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.21e-1

FS
type: SiteQuality
SIO_000300: 9.231999999999999e0

GenotypeQuality
all individuals: 792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3466
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49747
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4259
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 336
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66444
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.755e0

VQSLOD
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 9.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

FS
type: SiteQuality
SIO_000300: 6.414e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

DP
type: SiteQuality
SIO_000300: 1.573981e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 725
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49747
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3466
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505026789476853e-5
allele num: 66444
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.755e0

DP
type: SiteQuality
SIO_000300: 1.573981e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 9.82e0

FS
type: SiteQuality
SIO_000300: 6.414e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 436
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 335
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49658
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503623733197005e-5
allele num: 66506
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

DP
type: SiteQuality
SIO_000300: 1.574852e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.436e0

FS
type: SiteQuality
SIO_000300: 1.449e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.71e-1

QD
type: SiteQuality
SIO_000300: 1.243e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

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

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3465
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49736
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503352476021528e-5
allele num: 66518
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.16e-1

QD
type: SiteQuality
SIO_000300: 1.115e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 2.133e0

DP
type: SiteQuality
SIO_000300: 1.57492e6

VQSLOD
type: SiteQuality
SIO_000300: 9.56e-1

GenotypeQuality
all individuals: 334
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4253
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 791
bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.002e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 1.574137e6

MQRankSum
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 1.401e1

VQSLOD
type: SiteQuality
SIO_000300: -2.161e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.319e0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4252
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.214e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 4.047e0

DP
type: SiteQuality
SIO_000300: 1.573794e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.049e0

GenotypeQuality
all individuals: 87
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4251
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 102
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3451
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503668952243474e-5
allele num: 66504
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.61e-1

FS
type: SiteQuality
SIO_000300: 1.256e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 1.573077e6

QD
type: SiteQuality
SIO_000300: 1.454e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

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

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 461
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 434
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3436
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10150
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729804532087874e-4
allele num: 11562
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66504
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.25e-1

DP
type: SiteQuality
SIO_000300: 1.573004e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.25e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.861e0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3429
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.511142522029412e-5
allele num: 66502
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.059e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-2

DP
type: SiteQuality
SIO_000300: 1.573289e6

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.28e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
all individuals: 496
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4254
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 335
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.869719699960521e-5
allele num: 10132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66496
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 1.572595e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -5.331e-1

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4253
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 712
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007518796992481e-5
allele num: 66500
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.57272e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 6.121e0

QD
type: SiteQuality
SIO_000300: 1.41e1

VQSLOD
type: SiteQuality
SIO_000300: 8.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

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

GenotypeQuality
all individuals: 167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9986
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50652324565368e-5
allele num: 66378
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.17e1

MQ
type: SiteQuality
SIO_000300: 5.883e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 3.467e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.964e0

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

DP
type: SiteQuality
SIO_000300: 1.5662e6

VQSLOD
type: SiteQuality
SIO_000300: -7.916e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

GenotypeQuality
all individuals: 423
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
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variant carriers: 0

GenotypeQuality
all individuals: 3335
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4255
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212709192335678e-4
allele num: 16492
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.001803245842517e-4
allele num: 9982
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50652324565368e-5
allele num: 66378
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

FS
type: SiteQuality
SIO_000300: 9.64e-1

DP
type: SiteQuality
SIO_000300: 1.566442e6

QD
type: SiteQuality
SIO_000300: 1.445e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 48607
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 248
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GenotypeQuality
all individuals: 193
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GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 328
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variant carriers: 0

GenotypeQuality
all individuals: 4250
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510482750286992e-5
allele num: 66204
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.18e0

VQSLOD
type: SiteQuality
SIO_000300: -3.172e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.74e0

QD
type: SiteQuality
SIO_000300: 1.127e1

DP
type: SiteQuality
SIO_000300: 1.560642e6

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 326
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 70
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
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GenotypeQuality
all individuals: 82
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519202722411279e-5
allele num: 65824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.64e-1

FS
type: SiteQuality
SIO_000300: 3.757e0

VQSLOD
type: SiteQuality
SIO_000300: 6.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

DP
type: SiteQuality
SIO_000300: 1.549043e6

QD
type: SiteQuality
SIO_000300: 1.05e1

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeQuality
all individuals: 326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 3222
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GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 117
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GenotypeQuality
all individuals: 4264
bin: 9.75e1
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.672897196261682e-4
allele num: 6420
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.736061287772846e-4
allele num: 65788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.303e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.52e-1

DP
type: SiteQuality
SIO_000300: 1.547534e6

QD
type: SiteQuality
SIO_000300: 1.464e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

GenotypeQuality
all individuals: 383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 7.75e1
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GenotypeQuality
all individuals: 271
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variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.25e1
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GenotypeQuality
all individuals: 1783
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GenotypeQuality
all individuals: 4251
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2627
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GenotypeQuality
all individuals: 629
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GenotypeQuality
all individuals: 1620
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15992
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.830496064433462e-4
allele num: 10926
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.583681743316863e-5
allele num: 63144
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8040
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.316e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.81e-1

FS
type: SiteQuality
SIO_000300: 3.484e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-2

DP
type: SiteQuality
SIO_000300: 1.432974e6

QD
type: SiteQuality
SIO_000300: 1.474e1

MQ
type: SiteQuality
SIO_000300: 5.667e1

GenotypeQuality
all individuals: 37874
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7682
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 230
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1742
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2603
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10900
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.586495748191395e-5
allele num: 63032
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.692e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

DP
type: SiteQuality
SIO_000300: 1.423631e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

MQ
type: SiteQuality
SIO_000300: 5.291e1

QD
type: SiteQuality
SIO_000300: 1.117e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-1

GenotypeQuality
all individuals: 3314
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2125
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 659
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10604
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.093852548676438e-4
allele num: 9142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5996
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7718
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 1.309346e6

QD
type: SiteQuality
SIO_000300: 1.511e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.491e0

VQSLOD
type: SiteQuality
SIO_000300: 2.73e-1

FS
type: SiteQuality
SIO_000300: 1.849e0

GenotypeQuality
all individuals: 23587
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3923
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11299
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1980
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3657
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5840
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.633346400104534e-5
allele num: 61224
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7660
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15698
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.269599e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.878e0

QD
type: SiteQuality
SIO_000300: 5.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.572e0

GenotypeQuality
all individuals: 551
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4250
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 20860
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11536
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.699524133242692e-4
allele num: 5884
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.932263580165724e-5
allele num: 60824
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.33e-1

QD
type: SiteQuality
SIO_000300: 1.315e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.244218e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e0

GenotypeQuality
all individuals: 6634
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13199
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4845
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11146
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1626
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7326
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.879470460383324e-5
allele num: 10122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5724
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e0

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

QD
type: SiteQuality
SIO_000300: 2.892e1

VQSLOD
type: SiteQuality
SIO_000300: -3.811e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.953e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.179791e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

GenotypeQuality
all individuals: 4675
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7349
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1271
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 356
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variant carriers: 0

GenotypeQuality
all individuals: 413
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variant carriers: 0

GenotypeQuality
all individuals: 319
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variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2438
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.594566077552098e-5
allele num: 15164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7026
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.801e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.96e-1

QD
type: SiteQuality
SIO_000300: 1.135e1

FS
type: SiteQuality
SIO_000300: 3.699e0

VQSLOD
type: SiteQuality
SIO_000300: 5.19e-1

DP
type: SiteQuality
SIO_000300: 1.150752e6

GenotypeQuality
all individuals: 4781
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7333
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4747
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2736
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8643
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1202
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4705
bin: 9.75e1
variant carriers: 542

GenotypeQuality
all individuals: 493
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variant carriers: 4

GenotypeQuality
all individuals: 357
bin: 8.25e1
variant carriers: 7

GenotypeQuality
all individuals: 3206
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 433
allele frequency: 7.596757780974771e-3
allele num: 56998
num of homozygotes: 7

Other
type: Population
allele count: 3
allele frequency: 3.91644908616188e-3
allele num: 766
num of homozygotes: 0

Latino
type: Population
allele count: 33
allele frequency: 3.419689119170984e-3
allele num: 9650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6986
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.905976848570753e-4
allele num: 8466
num of homozygotes: 0

South Asian
type: Population
allele count: 76
allele frequency: 5.040456293938188e-3
allele num: 15078
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 3
allele frequency: 5.5005500550055e-4
allele num: 5454
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 1.154246e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-1

QD
type: SiteQuality
SIO_000300: 1.381e1

VQSLOD
type: SiteQuality
SIO_000300: 4.29e0

FS
type: SiteQuality
SIO_000300: 1.86e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 8194
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4759
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3309
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variant carriers: 0

GenotypeQuality
all individuals: 7381
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variant carriers: 0

GenotypeQuality
all individuals: 3245
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
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GenotypeQuality
all individuals: 230
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variant carriers: 0

GenotypeQuality
all individuals: 494
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variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.04777870913663e-4
allele num: 9544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.0e-3

MQ
type: SiteQuality
SIO_000300: 5.47e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.19e0

QD
type: SiteQuality
SIO_000300: 9.24e0

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.031e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

DP
type: SiteQuality
SIO_000300: 1.155088e6

GenotypeQuality
all individuals: 41298
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 806
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1551
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1469
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2116
bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65332
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.118451025056947e-5
allele num: 14048
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.462e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

VQSLOD
type: SiteQuality
SIO_000300: -3.775e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.845598e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

GenotypeQuality
all individuals: 1754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1068
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41315
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1482
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1943
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65416
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 2.117746717492588e-4
allele num: 14166
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 2.853219e6

FS
type: SiteQuality
SIO_000300: 1.786e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

QD
type: SiteQuality
SIO_000300: 1.229e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4